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Journal of Neurology

Volumn 247, Issue 12, 2000, Pages 968-969

Lack of α-synuclein gene mutations in families with autosomal dominant Parkinson's disease in Russia [2]

(5) Illarioshkin, S N a Ivanova Smolenskaya, I A a Markova, E D a Zagorovskaya, T B a Brice, A b

a RESEARCH CENTER OF NEUROLOGY (Russian Federation)

b INSERM (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; ALPHA SYNUCLEIN; DNA; GENE PRODUCT; HYDROLASE; THREONINE; UBIQUITIN;

AMINO ACID SUBSTITUTION; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 4Q; CLINICAL FEATURE; DEGENERATIVE DISEASE; GENE MUTATION; GENETIC ANALYSIS; GENETIC PREDISPOSITION; HUMAN; LETTER; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; RUSSIAN FEDERATION;

ADULT; AGED; ALPHA-SYNUCLEIN; CHROMOSOMES, HUMAN, PAIR 4; FAMILY HEALTH; HUMANS; MIDDLE AGED; MUTATION; NERVE TISSUE PROTEINS; PARKINSONIAN DISORDERS; RUSSIA; SYNUCLEINS;

EID: 0034524512 PISSN: 03405354 EISSN: None Source Type: Journal
DOI: 10.1007/s004150070056 Document Type: Letter

Times cited : (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.