. . . . . . . "[In a mitochondrial myopathy patient, a novel stop-codon mutation (G15761A) was found in the mitochondrial DNA (mtDNA) -encoded cytochrome b gene, resulting in loss of the last 41 amino acids of the protein and complex III deficiency]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:14:46+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .