9298830

Source:http://linkedlifedata.com/resource/pubmed/id/9298830

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0043157, umls-concept:C0043240, umls-concept:C0086418, umls-concept:C0205214, umls-concept:C0205314, umls-concept:C0268120, umls-concept:C0332307, umls-concept:C0374711, umls-concept:C0392360, umls-concept:C0439064, umls-concept:C0439659, umls-concept:C0679622, umls-concept:C1314939, umls-concept:C1511790, umls-concept:C1705181
pubmed:issue	3
pubmed:dateCreated	1997-10-29
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Adenine Phosphoribosyltransferase
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:AuerBB, pubmed-author:Hirsch-KauffmannMM, pubmed-author:KlockerHH, pubmed-author:MenardiCC, pubmed-author:Neuschmid-KasparFF, pubmed-author:SchneiderRR, pubmed-author:SchweigerMM
pubmed:issnType	Print
pubmed:volume	10
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	251-5
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:9298830-Adenine Phosphoribosyltransferase, pubmed-meshheading:9298830-Base Sequence, pubmed-meshheading:9298830-DNA Repair, pubmed-meshheading:9298830-European Continental Ancestry Group, pubmed-meshheading:9298830-Gene Amplification, pubmed-meshheading:9298830-Humans, pubmed-meshheading:9298830-Molecular Sequence Data, pubmed-meshheading:9298830-Mutation, pubmed-meshheading:9298830-Polymorphism, Restriction Fragment Length, pubmed-meshheading:9298830-Sequence Analysis, DNA, pubmed-meshheading:9298830-Templates, Genetic
pubmed:year	1997
pubmed:articleTitle	Human APRT deficiency: indication for multiple origins of the most common Caucasian mutation and detection of a novel type of mutation involving intrastrand-templated repair.
pubmed:affiliation	Institute of Biochemistry, University of Innsbruck, Austria.
pubmed:publicationType	Journal Article