16385265

Source:http://linkedlifedata.com/resource/pubmed/id/16385265

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0019425, umls-concept:C0205374, umls-concept:C0314657, umls-concept:C1112213, umls-concept:C1412070
pubmed:issue	1
pubmed:dateCreated	2005-12-30
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/16385265-16385246
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8211545
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/ABCB11 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/ATP-Binding Cassette Transporters, http://linkedlifedata.com/resource/pubmed/chemical/P-Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/multidrug resistance protein 3
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0277-2116
pubmed:author	pubmed-author:GirardMurielM, pubmed-author:HermeziuBogdanB, pubmed-author:JacqueminEmmanuelE, pubmed-author:LéonardClaudeC, pubmed-author:LyonnetStanislasS, pubmed-author:SanlavilleDamienD
pubmed:issnType	Print
pubmed:volume	42
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	114-6
pubmed:meshHeading	pubmed-meshheading:16385265-ATP-Binding Cassette Transporters, pubmed-meshheading:16385265-Cholestasis, pubmed-meshheading:16385265-Female, pubmed-meshheading:16385265-Gene Deletion, pubmed-meshheading:16385265-Genetic Predisposition to Disease, pubmed-meshheading:16385265-Humans, pubmed-meshheading:16385265-Infant, Newborn, pubmed-meshheading:16385265-Mutation, pubmed-meshheading:16385265-P-Glycoproteins, pubmed-meshheading:16385265-Risk Factors
pubmed:year	2006
pubmed:articleTitle	Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasis.
pubmed:affiliation	Pediatric Hepatology, Bicêtre University Hospital, Paris, France.
pubmed:publicationType	Journal Article, Case Reports