Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.

Wang, Jun-Ling; Jiang, Hong; Zhang, Shen; Xu, Qian; Zhou, Ya-Fang; Liao, Shu-Sheng; Shen, Lu; Yan, Xin-Xiang; Zhu, Huai-Xu; Pan, Qian; Xia, Kun; Tang, Bei-Sha

Wang, Jun-Ling; Jiang, Hong; Zhang, Shen; Xu, Qian; Zhou, Ya-Fang; Liao, Shu-Sheng; Shen, Lu; Yan, Xin-Xiang; Zhu, Huai-Xu; Pan, Qian; Xia, Kun; Tang, Bei-Sha.

J Genet ; 2008 Dec; 87(3): 283-6

Article in English | IMSEAR | ID: sea-114412

Subject(s)

Adolescent; Adult; Alleles; Asian People/genetics; Base Sequence; Blotting, Southern; Case-Control Studies; Child; Child, Preschool; China; DNA Mutational Analysis; Genetic Variation; Health; Humans; Microsatellite Repeats/genetics; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins/genetics; Spinocerebellar Ataxias/diagnosis

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Genetic Variation / Humans / DNA Mutational Analysis / Molecular Sequence Data / Base Sequence / Case-Control Studies / Child / Child, Preschool / China / Blotting, Southern Type of study: Diagnostic study / Observational study Country/Region as subject: Asia Language: English Journal: J Genet Year: 2008 Type: Article

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