Open AccessBroadening the phenotype of the m.5703G>A mutation in the mitochondrial tRNAAsn gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
Author(s) -
Jun Fu,
Ming Ma,
Ming Pang,
Lijian Yang,
Gang Li,
Jia Song,
Jiewen Zhang
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 - 10.1097/00029330-900000000-99933
Subject(s) - myoclonic epilepsy , mitochondrial myopathy , mitochondrial dna , genetics , mutation , gene , phenotype , biology , epilepsy , neuroscience