19762912

Source:http://linkedlifedata.com/resource/pubmed/id/19762912

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013421, umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0031437, umls-concept:C0035820, umls-concept:C0221032, umls-concept:C0439064, umls-concept:C1705535, umls-concept:C2827666
pubmed:issue	10
pubmed:dateCreated	2009-9-18
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985191R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/BSCL2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Protein gamma Subunits
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1468-330X
pubmed:author	pubmed-author:ChangY-CYC, pubmed-author:ChenS-TST, pubmed-author:ChungW-HWH, pubmed-author:HungS-ISI, pubmed-author:SunT QTQ, pubmed-author:YUY CYC
pubmed:issnType	Electronic
pubmed:volume	80
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1180-1
pubmed:meshHeading	pubmed-meshheading:19762912-Adult, pubmed-meshheading:19762912-Dystonic Disorders, pubmed-meshheading:19762912-Female, pubmed-meshheading:19762912-GTP-Binding Protein gamma Subunits, pubmed-meshheading:19762912-Humans, pubmed-meshheading:19762912-Lipodystrophy, Congenital Generalized, pubmed-meshheading:19762912-Male, pubmed-meshheading:19762912-Mental Disorders, pubmed-meshheading:19762912-Mutation, pubmed-meshheading:19762912-Phenotype, pubmed-meshheading:19762912-Taiwan
pubmed:year	2009
pubmed:articleTitle	Complementary mutations in seipin gene in a patient with Berardinelli-Seip congenital lipodystrophy and dystonia: phenotype variability suggests multiple roles of seipin gene.
pubmed:publicationType	Letter, Case Reports