12687460

Source:http://linkedlifedata.com/resource/pubmed/id/12687460

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0268164, umls-concept:C0336791, umls-concept:C0348026, umls-concept:C0796344, umls-concept:C1412290
pubmed:issue	5
pubmed:dateCreated	2003-5-8
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/12687460-12432429
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8708728
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0931-041X
pubmed:author	pubmed-author:HoppeBerndB, pubmed-author:KemperMarkusM, pubmed-author:LattaKayK, pubmed-author:RumsbyGillG, pubmed-author:von SchnakenburgChristianC
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	482-3; author reply 484
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:12687460-Genetic Testing, pubmed-meshheading:12687460-Humans, pubmed-meshheading:12687460-Hyperoxaluria, Primary
pubmed:year	2003
pubmed:articleTitle	Genetic analysis: a diagnostic tool for primary hyperoxaluria type 1.
pubmed:publicationType	Letter, Comment