Open AccessBrain atrophy in a patient with mitochondrial DNA G8363A mutation
Author(s) -
HongLiang Xu,
Yajun Lian,
Xin Chen
Publication year - 2019
Publication title -
chinese medical journal/chinese medical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 63
eISSN - 2542-5641
pISSN - 0366-6999
DOI - 10.1097/cm9.0000000000000395
Subject(s) - mitochondrial dna , atrophy , hearing loss , ataxia , medicine , sensorineural hearing loss , mitochondrial disease , weakness , mitochondrial encephalomyopathy , epilepsy , mitochondrial myopathy , pathology , genetics , audiology , surgery , biology , gene , psychiatry