SCOPUS 정보 검색 플랫폼

Volumn 242, Issue 4884, 1988, Pages 1427-1430

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

(8) Wallace, Douglas C a Singh, Gurparkash a Lott, Marie T a Hodge, Judy A a Schurr, Theodore G a Lezza, Angela M S a Elsas II, Louis J a Nikoskelainen, Eeva K b

a EMORY UNIVERSITY SCHOOL OF MEDICINE (United States)

b TURKU UNIVERSITY HOSPITAL (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE;

HEREDITARY OPTIC ATROPHY; HEREDITY; HUMAN; HUMAN CELL; MUTATION; PRIORITY JOURNAL;

ANIMAL; ARGININE; CAUCASOID RACE; CYTOCHROME REDUCTASES; DNA, MITOCHONDRIAL; FEMALE; GENES, STRUCTURAL; GEORGIA; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HISTIDINE; HUMAN; MACROMOLECULAR SYSTEMS; MALE; MUTATION; NADH DEHYDROGENASE; NEGROID RACE; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; REFERENCE VALUES; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0024242545 PISSN: 00368075 EISSN: None Source Type: Journal
DOI: 10.1126/science.3201231 Document Type: Article

Times cited : (2034)

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