Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Article Details

Citation

Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Science. 1988 Dec 9;242(4884):1427-30.

PubMed ID
3201231 [ View in PubMed
]
Abstract

Leber's hereditary optic neuropathy is a maternally inherited disease resulting in optic nerve degeneration and cardiac dysrhythmia. A mitochondrial DNA replacement mutation was identified that correlated with this disease in multiple families. This mutation converted a highly conserved arginine to a histidine at codon 340 in the NADH dehydrogenase subunit 4 gene and eliminated an Sfa NI site, thus providing a simple diagnostic test. This finding demonstrated that a nucleotide change in a mitochondrial DNA energy production gene can result in a neurological disease.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
NADH-ubiquinone oxidoreductase chain 4P03905Details
ATP synthase subunit aP00846Details