21154334

Source:http://linkedlifedata.com/resource/pubmed/id/21154334

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0152035, umls-concept:C0752125, umls-concept:C0796357
pubmed:issue	6
pubmed:dateCreated	2010-12-14
pubmed:abstractText	To characterize the clinical phenotype and the gene mutation of the spinocerebellar ataxia 7 (SCA7) family.
pubmed:language	chi
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9425197
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1003-9406
pubmed:author	pubmed-author:DuL CLC, pubmed-author:LeiJingJ, pubmed-author:LiHai-taoHT, pubmed-author:MaJian-huaJH, pubmed-author:ZhangXiao-ningXN
pubmed:issnType	Print
pubmed:volume	27
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	685-7
pubmed:meshHeading	pubmed-meshheading:21154334-Adult, pubmed-meshheading:21154334-Asian Continental Ancestry Group, pubmed-meshheading:21154334-Base Sequence, pubmed-meshheading:21154334-DNA Mutational Analysis, pubmed-meshheading:21154334-Female, pubmed-meshheading:21154334-Gene Frequency, pubmed-meshheading:21154334-Humans, pubmed-meshheading:21154334-Male, pubmed-meshheading:21154334-Molecular Sequence Data, pubmed-meshheading:21154334-Mutation, pubmed-meshheading:21154334-Pedigree, pubmed-meshheading:21154334-Spinocerebellar Ataxias, pubmed-meshheading:21154334-Young Adult
pubmed:year	2010
pubmed:articleTitle	[Mutation analysis of a Chinese family with spinocerebellar ataxia 7].
pubmed:affiliation	Department of Neurology, the First Teaching Hospital, Xinjiang Medical University, Urumqi, Xinjiang, P.R. China.
pubmed:publicationType	Journal Article, English Abstract, Research Support, Non-U.S. Gov't