19072839

Source:http://linkedlifedata.com/resource/pubmed/id/19072839

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0205210, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1826793, umls-concept:C2827447
pubmed:issue	3
pubmed:dateCreated	2009-1-15
pubmed:abstractText	To examine the gene mutation associated with clinical phenotype from a Chinese kindred with autosomal dominant hereditary spastic paraplegia (ADHSP).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8806914
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/REEP1 protein, human
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1098-2396
pubmed:author	pubmed-author:CheFeng YuanFY, pubmed-author:HSUJ YJY, pubmed-author:HengXue YuanXY, pubmed-author:HouSu JunSJ, pubmed-author:HuangShang ZhiSZ, pubmed-author:LiFei FengFF, pubmed-author:LiuShi EnSE, pubmed-author:LiuShi GuoSG, pubmed-author:LuDe Guode G, pubmed-author:WangHai PingHP, pubmed-author:WangQiangQ
pubmed:copyrightInfo	(c) 2008 Wiley-Liss, Inc.
pubmed:issnType	Electronic
pubmed:volume	63
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	201-5
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:19072839-Adolescent, pubmed-meshheading:19072839-Adult, pubmed-meshheading:19072839-Aged, pubmed-meshheading:19072839-Asian Continental Ancestry Group, pubmed-meshheading:19072839-DNA Mutational Analysis, pubmed-meshheading:19072839-Electric Stimulation, pubmed-meshheading:19072839-Electromyography, pubmed-meshheading:19072839-Evoked Potentials, Motor, pubmed-meshheading:19072839-Family Health, pubmed-meshheading:19072839-Female, pubmed-meshheading:19072839-Genetic Linkage, pubmed-meshheading:19072839-Humans, pubmed-meshheading:19072839-Magnetic Resonance Imaging, pubmed-meshheading:19072839-Male, pubmed-meshheading:19072839-Membrane Transport Proteins, pubmed-meshheading:19072839-Middle Aged, pubmed-meshheading:19072839-Mutation, pubmed-meshheading:19072839-Neural Conduction, pubmed-meshheading:19072839-Reaction Time, pubmed-meshheading:19072839-Spastic Paraplegia, Hereditary, pubmed-meshheading:19072839-Spinal Cord
pubmed:year	2009
pubmed:articleTitle	Clinical and genetic study of a novel mutation in the REEP1 gene.
pubmed:affiliation	Postgraduate School, Peking Union Medical College, Dong Cheng, Beijing.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't