An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathy

Biochemical and Biophysical Research Communications

Volumn 187, Issue 3, 1992, Pages 1551-1557

  Johns, Donald R ^a   Neufeld, Michael J ^a   Park, Raymond D ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HISTIDINE; METHIONINE; MITOCHONDRIAL DNA; TYROSINE; VALINE;

AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; GENE MUTATION; HAPLOTYPE; HEREDITARY OPTIC ATROPHY; HUMAN; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN DOMAIN;

BASE SEQUENCE; DNA, MITOCHONDRIAL; EVOLUTION; HAPLOTYPES; HUMAN; MOLECULAR SEQUENCE DATA; MUTATION; NADH DEHYDROGENASE; OLIGODEOXYRIBONUCLEOTIDES; OPTIC ATROPHIES, HEREDITARY; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026757115     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/0006-291X(92)90479-5     Document Type: Article

References (20)

1. Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation.