19050888

Source:http://linkedlifedata.com/resource/pubmed/id/19050888

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0205314, umls-concept:C0268243, umls-concept:C0332307, umls-concept:C0599155, umls-concept:C0679622, umls-concept:C1420259, umls-concept:C1556096
pubmed:issue	7
pubmed:dateCreated	2009-5-21
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9107334
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Sphingomyelin Phosphodiesterase
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1432-0584
pubmed:author	pubmed-author:ChenYing-FaYF, pubmed-author:LanMin-YuMY, pubmed-author:LinShyh-JerSJ, pubmed-author:LiuYu-FanYF, pubmed-author:PengCheng-HueiCH
pubmed:issnType	Electronic
pubmed:volume	88
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	695-7
pubmed:meshHeading	pubmed-meshheading:19050888-Adult, pubmed-meshheading:19050888-Bone Marrow Examination, pubmed-meshheading:19050888-Exons, pubmed-meshheading:19050888-Humans, pubmed-meshheading:19050888-Male, pubmed-meshheading:19050888-Mutation, Missense, pubmed-meshheading:19050888-Niemann-Pick Disease, Type B, pubmed-meshheading:19050888-Point Mutation, pubmed-meshheading:19050888-Sphingomyelin Phosphodiesterase, pubmed-meshheading:19050888-Taiwan
pubmed:year	2009
pubmed:articleTitle	A novel missense mutation of the SMPD1 gene in a Taiwanese patient with type B Niemann-Pick disease.
pubmed:publicationType	Letter, Case Reports