11483641

Source:http://linkedlifedata.com/resource/pubmed/id/11483641

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0018784, umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0597298, umls-concept:C0679622, umls-concept:C1418195
pubmed:issue	8
pubmed:dateCreated	2001-8-2
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/OTOF protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1468-6244
pubmed:author	pubmed-author:Al-GazaliL ILI, pubmed-author:BadinR ARA, pubmed-author:HousemanM JMJ, pubmed-author:JacksonA PAP, pubmed-author:MuellerR FRF, pubmed-author:RobertsEE
pubmed:issnType	Electronic
pubmed:volume	38
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	E25
pubmed:dateRevised	2008-11-20
pubmed:meshHeading	pubmed-meshheading:11483641-Base Sequence, pubmed-meshheading:11483641-DNA, pubmed-meshheading:11483641-DNA Mutational Analysis, pubmed-meshheading:11483641-Family Health, pubmed-meshheading:11483641-Hearing Loss, Sensorineural, pubmed-meshheading:11483641-Membrane Proteins, pubmed-meshheading:11483641-Mutation, pubmed-meshheading:11483641-Protein Isoforms
pubmed:year	2001
pubmed:articleTitle	A novel mutation in a family with non-syndromic sensorineural hearing loss that disrupts the newly characterised OTOF long isoforms.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't