A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Hanadi A. Abdelrahman; Aisha M. Al-Shamsi; Bassam R. Ali; Lihadh Al-Gazali

doi:10.1111/cge.13443

A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Research output: Contribution to journal › Letter › peer-review

30 Scopus citations

Original language	English
Pages (from-to)	586-587
Number of pages	2
Journal	Clinical Genetics
Volume	94
Issue number	6
DOIs	https://doi.org/10.1111/cge.13443
State	Published - Dec 2018

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10.1111/cge.13443

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title = "A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease",

author = "Abdelrahman, \{Hanadi A.\} and Al-Shamsi, \{Aisha M.\} and Ali, \{Bassam R.\} and Lihadh Al-Gazali",

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language = "English",

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T1 - A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

AU - Abdelrahman, Hanadi A.

AU - Al-Shamsi, Aisha M.

AU - Ali, Bassam R.

AU - Al-Gazali, Lihadh

PY - 2018/12

Y1 - 2018/12

UR - https://www.scopus.com/pages/publications/85054748482

U2 - 10.1111/cge.13443

DO - 10.1111/cge.13443

M3 - Letter

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AN - SCOPUS:85054748482

SN - 0009-9163

VL - 94

SP - 586

EP - 587

JO - Clinical Genetics

JF - Clinical Genetics

IS - 6

ER -

A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

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