10411712

Source:http://linkedlifedata.com/resource/pubmed/id/10411712

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C1418599, umls-concept:C1552961, umls-concept:C1853719
pubmed:issue	1
pubmed:dateCreated	1999-8-3
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/DK51034
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/10411712-10411677
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0323470
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/TRPP Cation Channels, http://linkedlifedata.com/resource/pubmed/chemical/polycystic kidney disease 1 protein
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0085-2538
pubmed:author	pubmed-author:Guay-WoodfordL MLM
pubmed:issnType	Print
pubmed:volume	56
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	344-6
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:10411712-Chromosome Mapping, pubmed-meshheading:10411712-Genetic Linkage, pubmed-meshheading:10411712-Humans, pubmed-meshheading:10411712-Mutation, pubmed-meshheading:10411712-Phenotype, pubmed-meshheading:10411712-Polycystic Kidney, Autosomal Dominant, pubmed-meshheading:10411712-Proteins, pubmed-meshheading:10411712-TRPP Cation Channels
pubmed:year	1999
pubmed:articleTitle	Phenotypic variability in PKD1: the family as a starting point.
pubmed:publicationType	Editorial, Comment, Research Support, U.S. Gov't, P.H.S., Review