12519376

Source:http://linkedlifedata.com/resource/pubmed/id/12519376

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011053, umls-concept:C0012634, umls-concept:C0017337, umls-concept:C0031437, umls-concept:C0439659, umls-concept:C0752354, umls-concept:C1300562, umls-concept:C1415938, umls-concept:C1421914, umls-concept:C1705535, umls-concept:C1824763, umls-concept:C1853760, umls-concept:C2828389, umls-concept:C2931689
pubmed:issue	1
pubmed:dateCreated	2003-1-9
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CNBP protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/myotonic dystrophy protein kinase
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0009-9163
pubmed:author	pubmed-author:BönschDD, pubmed-author:DeufelTT, pubmed-author:Lamprecht-DinnesenAA, pubmed-author:Lang-RothRR, pubmed-author:NeumannCC, pubmed-author:WitteOO
pubmed:issnType	Print
pubmed:volume	63
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	73-5
pubmed:dateRevised	2008-5-13
pubmed:meshHeading	pubmed-meshheading:12519376-Chromosome Mapping, pubmed-meshheading:12519376-Chromosomes, Human, Pair 3, pubmed-meshheading:12519376-Deafness, pubmed-meshheading:12519376-Humans, pubmed-meshheading:12519376-Myotonic Disorders, pubmed-meshheading:12519376-Protein-Serine-Threonine Kinases, pubmed-meshheading:12519376-RNA-Binding Proteins
pubmed:year	2003
pubmed:articleTitle	PROMM and deafness: exclusion of ZNF9 as the disease gene in DFNA18 suggests a polygenic origin of the PROMM/DM2 phenotype.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't