Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy [4]

American Journal of Human Genetics

Volumn 50, Issue 2, 1992, Pages 443-446

  Howell, N ^a   McCullough, D ^a   Bodis Wollner, I ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ADULT; AMINO ACID SUBSTITUTION; CASE REPORT; DIAGNOSIS; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN CELL; LETTER; MALE; PENETRANCE; PRIORITY JOURNAL;

ADULT; CASE REPORT; DNA, MITOCHONDRIAL; HUMAN; MALE; MUTATION; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POLYMERASE CHAIN REACTION; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0026499997     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)