Leber hereditary optic neuropathy: Identification of the same mitochondrial NDI mutation in six pedigrees

American Journal of Human Genetics

Volumn 49, Issue 5, 1991, Pages 939-950

  Howell, N ^a   Bindoff, L A ^a   McCullough, D A ^a   Kubacka, I ^a   Poulton, J ^a   Mackey, D ^a   Taylor, L ^a   Turnbull, D M ^a  

^a University of Texas Medical Branch School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

AMINO ACID SEQUENCE; ARTICLE; CLINICAL ARTICLE; ELECTRON TRANSPORT; FEMALE; GENE STRUCTURE; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; MITOCHONDRION; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; CLONING, MOLECULAR; FEMALE; HUMAN; MALE; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; MUTATION; NAD(P)H DEHYDROGENASE (QUINONE); NADH, NADPH OXIDOREDUCTASES; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0025944560     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)