19274735

Source:http://linkedlifedata.com/resource/pubmed/id/19274735

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0205214, umls-concept:C1384666, umls-concept:C1417557, umls-concept:C1514562, umls-concept:C1524003, umls-concept:C1838263, umls-concept:C1880389, umls-concept:C1883204, umls-concept:C1883221
pubmed:issue	4
pubmed:dateCreated	2009-3-31
pubmed:abstractText	To use clinical and genetic analyses to determine the mutation causing autosomal recessive nonsyndromic hearing loss (ARNSHL) segregating in two consanguineous Iranian families.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/R01 DC002842-15, http://linkedlifedata.com/resource/pubmed/grant/R01 DC003544-13, http://linkedlifedata.com/resource/pubmed/grant/R01 DCOO3544
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8607378
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/MYO15A protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Myosins
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1531-4995
pubmed:author	pubmed-author:ArzhanginySanazS, pubmed-author:BahloMelanieM, pubmed-author:HildebrandMichael SMS, pubmed-author:JalalvandKhadijehK, pubmed-author:KahriziKimiaK, pubmed-author:KimberlingWilliam JWJ, pubmed-author:MeyerNicole CNC, pubmed-author:NajmabadiHosseinH, pubmed-author:ShearerA EliotAE, pubmed-author:SmithRichard J HRJ, pubmed-author:StephanDietrichD, pubmed-author:WebsterJennifer AJA
pubmed:issnType	Electronic
pubmed:volume	119
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	727-33
pubmed:dateRevised	2011-6-13
pubmed:meshHeading	pubmed-meshheading:19274735-Chromosome Mapping, pubmed-meshheading:19274735-Chromosomes, Human, Pair 17, pubmed-meshheading:19274735-Consanguinity, pubmed-meshheading:19274735-Female, pubmed-meshheading:19274735-Genotype, pubmed-meshheading:19274735-Hearing Loss, Sensorineural, pubmed-meshheading:19274735-Humans, pubmed-meshheading:19274735-Iran, pubmed-meshheading:19274735-Lod Score, pubmed-meshheading:19274735-Male, pubmed-meshheading:19274735-Mutation, Missense, pubmed-meshheading:19274735-Myosins, pubmed-meshheading:19274735-Pedigree, pubmed-meshheading:19274735-Sequence Analysis, Protein
pubmed:year	2009
pubmed:articleTitle	Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.
pubmed:affiliation	Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City, Iowa 52242, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural