7520022

Source:http://linkedlifedata.com/resource/pubmed/id/7520022

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015295, umls-concept:C0017337, umls-concept:C0056889, umls-concept:C0599155
pubmed:issue	4
pubmed:dateCreated	1994-9-13
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0200525
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CFTR protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cystic Fibrosis Transmembrane..., http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins
pubmed:status	MEDLINE
pubmed:issn	0001-5652
pubmed:author	pubmed-author:GreifCC, pubmed-author:RosenkranzWW, pubmed-author:WagnerKK
pubmed:issnType	Print
pubmed:volume	44
pubmed:geneSymbol	CFTR
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	238-40
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:7520022-Base Sequence, pubmed-meshheading:7520022-Child, Preschool, pubmed-meshheading:7520022-Cystic Fibrosis, pubmed-meshheading:7520022-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:7520022-Exons, pubmed-meshheading:7520022-Female, pubmed-meshheading:7520022-Humans, pubmed-meshheading:7520022-Membrane Proteins, pubmed-meshheading:7520022-Molecular Sequence Data, pubmed-meshheading:7520022-Point Mutation
pubmed:articleTitle	A new missense mutation G1249E in exon 20 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
pubmed:affiliation	Institute of Medical Biology and Human Genetics, University of Graz, Austria.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't