10768629

Source:http://linkedlifedata.com/resource/pubmed/id/10768629

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0024408, umls-concept:C0030705, umls-concept:C0087012, umls-concept:C0152035, umls-concept:C0376249, umls-concept:C0439660, umls-concept:C0524894, umls-concept:C0598429, umls-concept:C0751781, umls-concept:C0752120, umls-concept:C0752121, umls-concept:C0752124, umls-concept:C0752125, umls-concept:C1540211, umls-concept:C1705387
pubmed:issue	4
pubmed:dateCreated	2000-4-27
pubmed:abstractText	To assess the frequency of SCA1 (spinocerebellar ataxia type 1), SCA2, SCA3/MJD (spinocerebellar ataxia type 3/Machado-Joseph disease), SCA6, SCA7, and DRPLA (dentatorubropallidoluysian atrophy) CAG trinucleotide repeat expansions [(CAG)n] among persons diagnosed with hereditary SCA from Chinese families.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ATXN3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/CACNA1A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SCA2 protein, http://linkedlifedata.com/resource/pubmed/chemical/ataxin-1, http://linkedlifedata.com/resource/pubmed/chemical/ataxin-7, http://linkedlifedata.com/resource/pubmed/chemical/atrophin-1
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0003-9942
pubmed:author	pubmed-author:DatSS, pubmed-author:JingLL, pubmed-author:LisMM, pubmed-author:OuyangSS, pubmed-author:PanQQ, pubmed-author:ShenLL, pubmed-author:TannII, pubmed-author:XiaJJ
pubmed:issnType	Print
pubmed:volume	57
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	540-4
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:10768629-Adolescent, pubmed-meshheading:10768629-Adult, pubmed-meshheading:10768629-Age of Onset, pubmed-meshheading:10768629-Alleles, pubmed-meshheading:10768629-Calcium Channels, pubmed-meshheading:10768629-Child, pubmed-meshheading:10768629-China, pubmed-meshheading:10768629-DNA Mutational Analysis, pubmed-meshheading:10768629-Gene Frequency, pubmed-meshheading:10768629-Genetic Predisposition to Disease, pubmed-meshheading:10768629-Genetic Testing, pubmed-meshheading:10768629-Humans, pubmed-meshheading:10768629-Middle Aged, pubmed-meshheading:10768629-Nerve Tissue Proteins, pubmed-meshheading:10768629-Nuclear Proteins, pubmed-meshheading:10768629-Proteins, pubmed-meshheading:10768629-Regression Analysis, pubmed-meshheading:10768629-Repressor Proteins, pubmed-meshheading:10768629-Severity of Illness Index, pubmed-meshheading:10768629-Spinocerebellar Ataxias, pubmed-meshheading:10768629-Trinucleotide Repeat Expansion
pubmed:year	2000
pubmed:articleTitle	Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
pubmed:affiliation	Department of Neurology, Xiangya Hospital, Hunan Medical University, People's Republic of China. neurogxm@public.cs.hn.cn
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't