Molecular and in silico investigation of a novel ECHS1 gene mutation in a consanguine family with short-chain enoyl-CoA hydratase deficiency and Mt-DNA depletion: effect on trimer assembly and catalytic activity
- Marwa Maalej
- , Lamia Sfaihi
- , Olfa Alila Fersi
- , Boudour Khabou
- , Marwa Ammar
- , Rahma Felhi
- , Marwa Kharrat
- , Jihen Chouchen
- , Thouraya Kammoun
- , Abdelaziz Tlili
- , Faiza Fakhfakh
- University of Sfax
- Faculty of Medecine of Sfax
Research output: Contribution to journal › Article › peer-review