Open AccessA meta-analysis and systematic review of Leigh syndrome: clinical manifestations, respiratory chain enzyme complex deficiency, and gene mutations
Author(s) -
Xueli Chang,
Yaxin Wu,
Jie Zhou,
Huaxing Meng,
Wei Zhang,
Junhong Guo
Publication year - 2020
Publication title -
medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 148
eISSN - 1536-5964
pISSN - 0025-7974
DOI - 10.1097/md.0000000000018634
Subject(s) - medicine , respiratory chain , mitochondrial respiratory chain , leigh disease , mitochondrial encephalomyopathies , mitochondrial dna , pathology , mitochondrial disease , gene mutation , mutation , genetics , mitochondrion , gene , mitochondrial myopathy , biology