15857421

Source:http://linkedlifedata.com/resource/pubmed/id/15857421

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008059, umls-concept:C0010674, umls-concept:C0019904, umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0056889, umls-concept:C0205210, umls-concept:C0205307, umls-concept:C0332120, umls-concept:C0596019, umls-concept:C1327616, umls-concept:C1524003, umls-concept:C1999230
pubmed:issue	6
pubmed:dateCreated	2005-4-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CFTR protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cystic Fibrosis Transmembrane...
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0009-9163
pubmed:author	pubmed-author:BallmannMM, pubmed-author:DerichsNN, pubmed-author:ErnstingAA, pubmed-author:GallatiSS, pubmed-author:GrundII, pubmed-author:Körtge-JungSS, pubmed-author:KozlowskiPP, pubmed-author:SchusterAA, pubmed-author:StolpeCC, pubmed-author:StuhrmannMM
pubmed:issnType	Print
pubmed:volume	67
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	529-31
pubmed:dateRevised	2005-11-17
pubmed:meshHeading	pubmed-meshheading:15857421-Child, Preschool, pubmed-meshheading:15857421-Cystic Fibrosis, pubmed-meshheading:15857421-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:15857421-Female, pubmed-meshheading:15857421-Homozygote, pubmed-meshheading:15857421-Humans, pubmed-meshheading:15857421-Male, pubmed-meshheading:15857421-Mutation, pubmed-meshheading:15857421-Pedigree, pubmed-meshheading:15857421-Phenotype
pubmed:year	2005
pubmed:articleTitle	Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this cystic fibrosis transmembrane conductance regulator mutation does not cause cystic fibrosis.
pubmed:publicationType	Letter, Case Reports