De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome-Reference-Cited by-同舟云学术

De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome

Published:2023-04 Issue: Volume:860 Page:147229
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Lou Xiaoting,Zhou Yuwei,Liu Zhimei,Xie Yaojun,Zhang Luyi,Zhao Suzhou,Gong Shuai,Zhuo Xiuwei,Wang Junling,Dai Lifang,Ren Xiaotun,Tong Xiao,Jiang Liangliang,Fang Hezhi,Fang Fang,Lyu Jianxin

Publisher

Elsevier BV

Subject

Genetics,General Medicine

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5. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options;El-Hattab;Mol. Genet. Metab.,2015

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