Spinocerebellar ataxia type 1 in China molecular analysis and Genotype-Phenotype correlation in 5 families

Archives of Neurology

Volumn 58, Issue 5, 2001, Pages 789-794

  Zhou, Yong Xing ^a,b,c   Qiao, Wen Hui ^c   Gu, Wei Hong ^a   Xie, Heng ^d   Tang, Bei Sha ^e   Zhou, Lian Sheng ^f   Yang, Bin Xian ^a   Takiyama, Yoshihisa ^g   Tsuji, Shoji ^h   He, Hui Yu ^a   Deng, Chu Xia ^c   Goldfarb, Lev G ^b   Wang, Guo Xiang ^a  

^a CHINA JAPAN FRIENDSHIP HOSPITAL   (China)

^b NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

^d NATIONAL CANCER INSTITUTE   (United States)

^e CENTRAL SOUTH UNIVERSITY   (China)

^f Oriental People's Hospital of Xuzhou   (China)

^g JICHI MEDICAL UNIVERSITY   (Japan)

^h NIIGATA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHINA; CHROMOSOME ANALYSIS; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENOME; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; PHENOTYPE; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPASTIC PARAPLEGIA; SPINOCEREBELLAR DEGENERATION;

EID: 0035004822     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.58.5.789     Document Type: Article

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