The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation
published in: Human Molecular Genetics
date of publication: 2015-12-08
main subject: mitochondrial DNA
Cites articles 54
- 2008-11-10
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Article - wd:Q38813517