A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations

Ammar, M; Safi, W; Tlili, A; Alila-Fersi, O; Frikha, F; Chouchen, J; Mnif, F; Kharrat, M; Maalej, M; Felhi, R; Abid, M; Mnif-Feki, M; Kacem, FH; Fakhfakh, F; Mkaouar-Rebai, E

Fakhfakh, F (通讯作者),Fac Sci Sfax, Lab Mol & Funct Genet, Route Soukra Km 3, Sfax, Tunisia.

INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2022; 82 (7): 626

Abstract

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE; OMIM 603041) is a rare inherited metabolic disorder mostly caused by mutations in TYMP g......

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