Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.
dc.contributor.author | Wang, Jun-Ling | en_US |
dc.contributor.author | Jiang, Hong | en_US |
dc.contributor.author | Zhang, Shen | en_US |
dc.contributor.author | Xu, Qian | en_US |
dc.contributor.author | Zhou, Ya-Fang | en_US |
dc.contributor.author | Liao, Shu-Sheng | en_US |
dc.contributor.author | Shen, Lu | en_US |
dc.contributor.author | Yan, Xin-Xiang | en_US |
dc.contributor.author | Zhu, Huai-Xu | en_US |
dc.contributor.author | Pan, Qian | en_US |
dc.contributor.author | Xia, Kun | en_US |
dc.contributor.author | Tang, Bei-Sha | en_US |
dc.date.accessioned | 2008-12-17 | en_US |
dc.date.accessioned | 2009-06-02T07:22:43Z | |
dc.date.available | 2008-12-17 | en_US |
dc.date.available | 2009-06-02T07:22:43Z | |
dc.date.issued | 2008-12-17 | en_US |
dc.description.affiliation | Department of Neurology, Xiangya Hospital, Central South University, Changsha 410008, People's Republic of China. | en_US |
dc.identifier.citation | Wang JL, Jiang H, Zhang S, Xu Q, Zhou YF, Liao SS, Shen L, Yan XX, Zhu HX, Pan Q, Xia K, Tang BS. Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han. Journal of Genetics. 2008 Dec; 87(3): 283-6 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/114412 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://www.ias.ac.in/jgenet/index.html | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Alleles | en_US |
dc.subject.mesh | Asian Continental Ancestry Group --genetics | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Blotting, Southern | en_US |
dc.subject.mesh | Case-Control Studies | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Child, Preschool | en_US |
dc.subject.mesh | China | en_US |
dc.subject.mesh | DNA Mutational Analysis | en_US |
dc.subject.mesh | Genetic Variation | en_US |
dc.subject.mesh | Health | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Microsatellite Repeats --genetics | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Nerve Tissue Proteins --genetics | en_US |
dc.subject.mesh | Spinocerebellar Ataxias --diagnosis | en_US |
dc.title | Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han. | en_US |
dc.type | Journal Article | en_US |
dc.type | Research Support, Non-U.S. Gov't | en_US |
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