Systematic analysis of a mitochondrial disease-causing ND6 mutation in mitochondrial deficiency.
Chen D, Zhao Q, Xiong J, Lou X, Han Q, Wei X, Xie J, Li X, Zhou H, Shen L, Yang Y, Fang H, Lyu J.
Chen D, et al. Among authors: yang y.
Mol Genet Genomic Med. 2020 May;8(5):e1199. doi: 10.1002/mgg3.1199. Epub 2020 Mar 12.
Mol Genet Genomic Med. 2020.
PMID: 32162843
Free PMC article.