SCOPUS 정보 검색 플랫폼

Volumn 54, Issue 20, 1994, Pages 1459-1464

Trinucleotide repeats in neurologic diseases: An hypothesis concerning the pathogenesis of Huntington's disease, Kennedy's disease, and spinocerebellar ataxia type I

(2) Cha, Jang Ho J a Dure IV, Leon S a

a MASSACHUSETTS GENERAL HOSPITAL (United States)

Author keywords

genetic abnormalities; Huntington's disease; Kennedy's disease; trinucleotide repeat

Indexed keywords

PROTEIN; TRINUCLEOTIDE;

ATAXIA; ENERGY METABOLISM; GENETIC DISORDER; HUMAN; HUNTINGTON CHOREA; HYPOTHESIS; MUSCLE ATROPHY; NERVE DEGENERATION; NEUROLOGIC DISEASE; NEUROTOXICITY; SHORT SURVEY; SPINOCEREBELLAR DEGENERATION;

BASE SEQUENCE; CENTRAL NERVOUS SYSTEM; HUMAN; HUNTINGTON DISEASE; MODELS, NEUROLOGICAL; MUSCULAR ATROPHY, SPINAL; NERVE TISSUE PROTEINS; NEURONS; REPETITIVE SEQUENCES, NUCLEIC ACID; SPINOCEREBELLAR DEGENERATIONS; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028220405 PISSN: 00243205 EISSN: None Source Type: Journal
DOI: 10.1016/0024-3205(94)90012-4 Document Type: Article

Times cited : (29)

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