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

dc.contributor.authorWang, Jun-Lingen_US
dc.contributor.authorJiang, Hongen_US
dc.contributor.authorZhang, Shenen_US
dc.contributor.authorXu, Qianen_US
dc.contributor.authorZhou, Ya-Fangen_US
dc.contributor.authorLiao, Shu-Shengen_US
dc.contributor.authorShen, Luen_US
dc.contributor.authorYan, Xin-Xiangen_US
dc.contributor.authorZhu, Huai-Xuen_US
dc.contributor.authorPan, Qianen_US
dc.contributor.authorXia, Kunen_US
dc.contributor.authorTang, Bei-Shaen_US
dc.date.accessioned2008-12-17en_US
dc.date.accessioned2009-06-02T07:22:43Z
dc.date.available2008-12-17en_US
dc.date.available2009-06-02T07:22:43Z
dc.date.issued2008-12-17en_US
dc.description.affiliationDepartment of Neurology, Xiangya Hospital, Central South University, Changsha 410008, People's Republic of China.en_US
dc.identifier.citationWang 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): 283-6en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/114412
dc.language.isoengen_US
dc.source.urihttps://www.ias.ac.in/jgenet/index.htmlen_US
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshAllelesen_US
dc.subject.meshAsian Continental Ancestry Group --geneticsen_US
dc.subject.meshBase Sequenceen_US
dc.subject.meshBlotting, Southernen_US
dc.subject.meshCase-Control Studiesen_US
dc.subject.meshChilden_US
dc.subject.meshChild, Preschoolen_US
dc.subject.meshChinaen_US
dc.subject.meshDNA Mutational Analysisen_US
dc.subject.meshGenetic Variationen_US
dc.subject.meshHealthen_US
dc.subject.meshHumansen_US
dc.subject.meshMicrosatellite Repeats --geneticsen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshMolecular Sequence Dataen_US
dc.subject.meshNerve Tissue Proteins --geneticsen_US
dc.subject.meshSpinocerebellar Ataxias --diagnosisen_US
dc.titleLack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.en_US
dc.typeJournal Articleen_US
dc.typeResearch Support, Non-U.S. Gov'ten_US
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