Broadening the phenotype of m.5703G > A mutation in mitochondrial tRNAAsn gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome.

Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNAAsn gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome.
Chin Med J (Engl). 2019 Apr 05;132(7):865-867
Authors: Fu J, Ma MM, Pang M, Yang L, Li G, Song J, Zhang JW
PMID: 30897601 [PubMed - in process]

Source: Chinese Medical Journal - March 22, 2019 Category: General Medicine Authors: Fu J, Ma MM, Pang M, Yang L, Li G, Song J, Zhang JW Tags: Chin Med J (Engl) Source Type: research