17531128

Source:http://linkedlifedata.com/resource/pubmed/id/17531128

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0016504, umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0037773, umls-concept:C0152035, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1420348, umls-concept:C1551910, umls-concept:C2931355
pubmed:issue	9
pubmed:dateCreated	2007-5-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7513795
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ATL1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/GTP Phosphohydrolases, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0366-6999
pubmed:author	pubmed-author:ChenSu-qinSQ, pubmed-author:GuoHuiH, pubmed-author:LiXun-huaXH, pubmed-author:LiangYin-xingYX, pubmed-author:SongChunC, pubmed-author:WangYi-mingYM, pubmed-author:YangZhi-yunZY, pubmed-author:ZhouChun-longCL, pubmed-author:ZhouYanY
pubmed:issnType	Print
pubmed:day	5
pubmed:volume	120
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	834-7
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:17531128-Adolescent, pubmed-meshheading:17531128-Adult, pubmed-meshheading:17531128-Aged, pubmed-meshheading:17531128-Child, pubmed-meshheading:17531128-Child, Preschool, pubmed-meshheading:17531128-China, pubmed-meshheading:17531128-Evoked Potentials, Somatosensory, pubmed-meshheading:17531128-Evolution, Molecular, pubmed-meshheading:17531128-Female, pubmed-meshheading:17531128-Foot Deformities, Congenital, pubmed-meshheading:17531128-GTP Phosphohydrolases, pubmed-meshheading:17531128-GTP-Binding Proteins, pubmed-meshheading:17531128-Genes, Dominant, pubmed-meshheading:17531128-Humans, pubmed-meshheading:17531128-Male, pubmed-meshheading:17531128-Membrane Proteins, pubmed-meshheading:17531128-Middle Aged, pubmed-meshheading:17531128-Mutation, pubmed-meshheading:17531128-Spastic Paraplegia, Hereditary
pubmed:year	2007
pubmed:articleTitle	A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family.
pubmed:affiliation	Department of Neurology, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, 510089, China.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't