Correction to: Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2)

Shams Anazi; Sateesh Maddirevula; Vincenzo Salpietro; Yasmine T. Asi; Saud Alsahli; Amal Alhashem; Hanan E. Shamseldin; Fatema AlZahrani; Nisha Patel; Niema Ibrahim; Firdous M. Abdulwahab; Mais Hashem; Nadia Alhashmi; Fathiya Al Murshedi; Adila Al Kindy; Ahmad Alshaer; Ahmed Rumayyan; Saeed Al Tala; Wesam Kurdi; Abdulaziz Alsaman; Ali Alasmari; Selina Banu; Tipu Sultan; Mohammed M. Saleh; Hisham Alkuraya; Mustafa A. Salih; Hesham Aldhalaan; Tawfeg Ben-Omran; Fatima Al Musafri; Rehab Ali; Jehan Suleiman; Brahim Tabarki; Ayman W. El-Hattab; Caleb Bupp; Majid Alfadhel; Nada Al Tassan; Dorota Monies; Stefan T. Arold; Mohamed Abouelhoda; Tammaryn Lashley; Henry Houlden; Eissa Faqeih; Fowzan S. Alkuraya

doi:10.1007/s00439-017-1859-7

Correction to: Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2)

Shams Anazi
, Sateesh Maddirevula
, Vincenzo Salpietro
, Yasmine T. Asi
, Saud Alsahli
, Amal Alhashem
, Hanan E. Shamseldin
, Fatema AlZahrani
, Nisha Patel
, Niema Ibrahim
, Firdous M. Abdulwahab
, Mais Hashem
, Nadia Alhashmi
, Fathiya Al Murshedi
, Adila Al Kindy
, Ahmad Alshaer
, Ahmed Rumayyan
, Saeed Al Tala
, Wesam Kurdi
, Abdulaziz Alsaman

Ali Alasmari, Selina Banu, Tipu Sultan, Mohammed M. Saleh, Hisham Alkuraya, Mustafa A. Salih, Hesham Aldhalaan, Tawfeg Ben-Omran, Fatima Al Musafri, Rehab Ali, Jehan Suleiman, Brahim Tabarki, Ayman W. El-Hattab, Caleb Bupp, Majid Alfadhel, Nada Al Tassan, Dorota Monies, Stefan T. Arold, Mohamed Abouelhoda, Tammaryn Lashley, Henry Houlden, Eissa Faqeih, Fowzan S. Alkuraya

King Faisal Specialist Hospital and Research Centre
University College London
Prince Sultan Military Medical City
Sultan Qaboos University
King Saud bin Abdulaziz University for Health Sciences
King Abdulaziz Medical City - Riyadh
King Fahad Medical City
ICH and SSF Hospital Mirpur
Children’s Hospital and Institute of Child Health
Specialized Medical Centre Hospital
King Saud University
Hamad Medical Corporation
Spectrum Health
King Abdulaziz City for Science and Technology
King Abdullah University of Science and Technology

Research output: Contribution to journal › Comment/debate

6 Scopus citations

Abstract

Variant nomenclature discrepancy was identified in the article “Expanding the genetic heterogeneity of intellectual disability”, Human Genetics, November 2017, Volume 136, Issue 11-12, pp 1419-1429 after its publication. Specifically, the nomenclature of GTF3C3 was originally listed as NM_012086.4:c.1382+3A>G when it should be NM_012086.4:c.1390+3A>G, the nomenclature of MADD was originally listed as NM_001135943.1:c.2930T>G:p.(Val977Gly) when it should be NM_001135943.1:c.2930T>G:p.(Leu977Arg), and the variant NM_001164416.1:c.124C>T:p.(Arg42*) was listed under the gene's name VWA3B when it should be H2BFM. The following changes were made in the attached corrections: 1. Nomenclature of GTF3C3 is changed to NM_012086.4:c.1390+3A>G in 15DG0315 (from NM_012086.4:c.1382+3A>G) in the main text, Table S1, Table S2 and Figure S1. 2. The variant NM_001164416.1:c.124C>T:p.(Arg42*) in 17DG0782 is now correctly listed under the name H2BFM in the abstract, Table 1, Table S1 and Table S2. 3. Nomenclature of MADD is changed to NM_001135943.1:c.2930T>G:p.(Leu977Arg) in 17DG0771 (From NM_001135943.1:c.2930T>G:p. (Val977Gly) in results, Table 1, Table S1, and Table S2. The authors sincerely apologize for these errors and appreciate the opportunity to mend the records.

Original language	English
Pages (from-to)	105-109
Number of pages	5
Journal	Human Genetics
Volume	137
Issue number	1
DOIs	https://doi.org/10.1007/s00439-017-1859-7
State	Published - 1 Jan 2018

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Anazi, S., Maddirevula, S., Salpietro, V., Asi, Y. T., Alsahli, S., Alhashem, A., Shamseldin, H. E., AlZahrani, F., Patel, N., Ibrahim, N., Abdulwahab, F. M., Hashem, M., Alhashmi, N., Al Murshedi, F., Al Kindy, A., Alshaer, A., Rumayyan, A., Al Tala, S., Kurdi, W., ... Alkuraya, F. S. (2018). Correction to: Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2). Human Genetics, 137(1), 105-109. https://doi.org/10.1007/s00439-017-1859-7

@article{dad093f08f7c487098afead6d2a08003,

title = "Correction to: Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2)",

abstract = "Variant nomenclature discrepancy was identified in the article “Expanding the genetic heterogeneity of intellectual disability”, Human Genetics, November 2017, Volume 136, Issue 11-12, pp 1419-1429 after its publication. Specifically, the nomenclature of GTF3C3 was originally listed as NM\_012086.4:c.1382+3A>G when it should be NM\_012086.4:c.1390+3A>G, the nomenclature of MADD was originally listed as NM\_001135943.1:c.2930T>G:p.(Val977Gly) when it should be NM\_001135943.1:c.2930T>G:p.(Leu977Arg), and the variant NM\_001164416.1:c.124C>T:p.(Arg42*) was listed under the gene's name VWA3B when it should be H2BFM. The following changes were made in the attached corrections: 1. Nomenclature of GTF3C3 is changed to NM\_012086.4:c.1390+3A>G in 15DG0315 (from NM\_012086.4:c.1382+3A>G) in the main text, Table S1, Table S2 and Figure S1. 2. The variant NM\_001164416.1:c.124C>T:p.(Arg42*) in 17DG0782 is now correctly listed under the name H2BFM in the abstract, Table 1, Table S1 and Table S2. 3. Nomenclature of MADD is changed to NM\_001135943.1:c.2930T>G:p.(Leu977Arg) in 17DG0771 (From NM\_001135943.1:c.2930T>G:p. (Val977Gly) in results, Table 1, Table S1, and Table S2. The authors sincerely apologize for these errors and appreciate the opportunity to mend the records.",

author = "Shams Anazi and Sateesh Maddirevula and Vincenzo Salpietro and Asi, \{Yasmine T.\} and Saud Alsahli and Amal Alhashem and Shamseldin, \{Hanan E.\} and Fatema AlZahrani and Nisha Patel and Niema Ibrahim and Abdulwahab, \{Firdous M.\} and Mais Hashem and Nadia Alhashmi and \{Al Murshedi\}, Fathiya and \{Al Kindy\}, Adila and Ahmad Alshaer and Ahmed Rumayyan and \{Al Tala\}, Saeed and Wesam Kurdi and Abdulaziz Alsaman and Ali Alasmari and Selina Banu and Tipu Sultan and Saleh, \{Mohammed M.\} and Hisham Alkuraya and Salih, \{Mustafa A.\} and Hesham Aldhalaan and Tawfeg Ben-Omran and \{Al Musafri\}, Fatima and Rehab Ali and Jehan Suleiman and Brahim Tabarki and El-Hattab, \{Ayman W.\} and Caleb Bupp and Majid Alfadhel and \{Al Tassan\}, Nada and Dorota Monies and Arold, \{Stefan T.\} and Mohamed Abouelhoda and Tammaryn Lashley and Henry Houlden and Eissa Faqeih and Alkuraya, \{Fowzan S.\}",

note = "Publisher Copyright: {\textcopyright} 2017, Springer-Verlag GmbH Germany, part of Springer Nature.",

year = "2018",

month = jan,

day = "1",

doi = "10.1007/s00439-017-1859-7",

language = "English",

volume = "137",

pages = "105--109",

journal = "Human Genetics",

issn = "0340-6717",

publisher = "Springer Science and Business Media Deutschland GmbH",

number = "1",

}

Anazi, S, Maddirevula, S, Salpietro, V, Asi, YT, Alsahli, S, Alhashem, A, Shamseldin, HE, AlZahrani, F, Patel, N, Ibrahim, N, Abdulwahab, FM, Hashem, M, Alhashmi, N, Al Murshedi, F, Al Kindy, A, Alshaer, A, Rumayyan, A, Al Tala, S, Kurdi, W, Alsaman, A, Alasmari, A, Banu, S, Sultan, T, Saleh, MM, Alkuraya, H, Salih, MA, Aldhalaan, H, Ben-Omran, T, Al Musafri, F, Ali, R, Suleiman, J, Tabarki, B, El-Hattab, AW, Bupp, C, Alfadhel, M, Al Tassan, N, Monies, D, Arold, ST, Abouelhoda, M, Lashley, T, Houlden, H, Faqeih, E & Alkuraya, FS 2018, 'Correction to: Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2)', Human Genetics, vol. 137, no. 1, pp. 105-109. https://doi.org/10.1007/s00439-017-1859-7

TY - JOUR

T1 - Correction to

T2 - Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2)

AU - Anazi, Shams

AU - Maddirevula, Sateesh

AU - Salpietro, Vincenzo

AU - Asi, Yasmine T.

AU - Alsahli, Saud

AU - Alhashem, Amal

AU - Shamseldin, Hanan E.

AU - AlZahrani, Fatema

AU - Patel, Nisha

AU - Ibrahim, Niema

AU - Abdulwahab, Firdous M.

AU - Hashem, Mais

AU - Alhashmi, Nadia

AU - Al Murshedi, Fathiya

AU - Al Kindy, Adila

AU - Alshaer, Ahmad

AU - Rumayyan, Ahmed

AU - Al Tala, Saeed

AU - Kurdi, Wesam

AU - Alsaman, Abdulaziz

AU - Alasmari, Ali

AU - Banu, Selina

AU - Sultan, Tipu

AU - Saleh, Mohammed M.

AU - Alkuraya, Hisham

AU - Salih, Mustafa A.

AU - Aldhalaan, Hesham

AU - Ben-Omran, Tawfeg

AU - Al Musafri, Fatima

AU - Ali, Rehab

AU - Suleiman, Jehan

AU - Tabarki, Brahim

AU - El-Hattab, Ayman W.

AU - Bupp, Caleb

AU - Alfadhel, Majid

AU - Al Tassan, Nada

AU - Monies, Dorota

AU - Arold, Stefan T.

AU - Abouelhoda, Mohamed

AU - Lashley, Tammaryn

AU - Houlden, Henry

AU - Faqeih, Eissa

AU - Alkuraya, Fowzan S.

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Variant nomenclature discrepancy was identified in the article “Expanding the genetic heterogeneity of intellectual disability”, Human Genetics, November 2017, Volume 136, Issue 11-12, pp 1419-1429 after its publication. Specifically, the nomenclature of GTF3C3 was originally listed as NM_012086.4:c.1382+3A>G when it should be NM_012086.4:c.1390+3A>G, the nomenclature of MADD was originally listed as NM_001135943.1:c.2930T>G:p.(Val977Gly) when it should be NM_001135943.1:c.2930T>G:p.(Leu977Arg), and the variant NM_001164416.1:c.124C>T:p.(Arg42*) was listed under the gene's name VWA3B when it should be H2BFM. The following changes were made in the attached corrections: 1. Nomenclature of GTF3C3 is changed to NM_012086.4:c.1390+3A>G in 15DG0315 (from NM_012086.4:c.1382+3A>G) in the main text, Table S1, Table S2 and Figure S1. 2. The variant NM_001164416.1:c.124C>T:p.(Arg42*) in 17DG0782 is now correctly listed under the name H2BFM in the abstract, Table 1, Table S1 and Table S2. 3. Nomenclature of MADD is changed to NM_001135943.1:c.2930T>G:p.(Leu977Arg) in 17DG0771 (From NM_001135943.1:c.2930T>G:p. (Val977Gly) in results, Table 1, Table S1, and Table S2. The authors sincerely apologize for these errors and appreciate the opportunity to mend the records.

AB - Variant nomenclature discrepancy was identified in the article “Expanding the genetic heterogeneity of intellectual disability”, Human Genetics, November 2017, Volume 136, Issue 11-12, pp 1419-1429 after its publication. Specifically, the nomenclature of GTF3C3 was originally listed as NM_012086.4:c.1382+3A>G when it should be NM_012086.4:c.1390+3A>G, the nomenclature of MADD was originally listed as NM_001135943.1:c.2930T>G:p.(Val977Gly) when it should be NM_001135943.1:c.2930T>G:p.(Leu977Arg), and the variant NM_001164416.1:c.124C>T:p.(Arg42*) was listed under the gene's name VWA3B when it should be H2BFM. The following changes were made in the attached corrections: 1. Nomenclature of GTF3C3 is changed to NM_012086.4:c.1390+3A>G in 15DG0315 (from NM_012086.4:c.1382+3A>G) in the main text, Table S1, Table S2 and Figure S1. 2. The variant NM_001164416.1:c.124C>T:p.(Arg42*) in 17DG0782 is now correctly listed under the name H2BFM in the abstract, Table 1, Table S1 and Table S2. 3. Nomenclature of MADD is changed to NM_001135943.1:c.2930T>G:p.(Leu977Arg) in 17DG0771 (From NM_001135943.1:c.2930T>G:p. (Val977Gly) in results, Table 1, Table S1, and Table S2. The authors sincerely apologize for these errors and appreciate the opportunity to mend the records.

UR - https://www.scopus.com/pages/publications/85039721667

U2 - 10.1007/s00439-017-1859-7

DO - 10.1007/s00439-017-1859-7

M3 - Comment/debate

C2 - 29288388

AN - SCOPUS:85039721667

SN - 0340-6717

VL - 137

SP - 105

EP - 109

JO - Human Genetics

JF - Human Genetics

IS - 1

ER -

Correction to: Expanding the genetic heterogeneity of intellectual disability (Human Genetics, (2017), 136, 11-12, (1419-1429), 10.1007/s00439-017-1843-2)

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