9500541

Source:http://linkedlifedata.com/resource/pubmed/id/9500541

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011053, umls-concept:C0015127, umls-concept:C0026882, umls-concept:C0271829, umls-concept:C1314792, umls-concept:C1418445, umls-concept:C1419060
pubmed:issue	3
pubmed:dateCreated	1998-3-30
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/Z01DC00026
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9216904
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SLC26A4 protein, human
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1061-4036
pubmed:author	pubmed-author:DesmukhDD, pubmed-author:EverettL ALA, pubmed-author:FriedmanT BTB, pubmed-author:GreenE DED, pubmed-author:LalwaniA KAK, pubmed-author:LiX CXC, pubmed-author:WilcoxE RER
pubmed:issnType	Print
pubmed:volume	18
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	215-7
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:9500541-Adolescent, pubmed-meshheading:9500541-Adult, pubmed-meshheading:9500541-Amino Acid Sequence, pubmed-meshheading:9500541-Carrier Proteins, pubmed-meshheading:9500541-Child, pubmed-meshheading:9500541-Child, Preschool, pubmed-meshheading:9500541-Chromosomes, Human, Pair 7, pubmed-meshheading:9500541-Cochlea, pubmed-meshheading:9500541-Female, pubmed-meshheading:9500541-Genes, Recessive, pubmed-meshheading:9500541-Genetic Linkage, pubmed-meshheading:9500541-Genetic Markers, pubmed-meshheading:9500541-Goiter, pubmed-meshheading:9500541-Hearing Loss, Sensorineural, pubmed-meshheading:9500541-Homozygote, pubmed-meshheading:9500541-Humans, pubmed-meshheading:9500541-Male, pubmed-meshheading:9500541-Membrane Transport Proteins, pubmed-meshheading:9500541-Molecular Sequence Data, pubmed-meshheading:9500541-Mutation, pubmed-meshheading:9500541-Pedigree, pubmed-meshheading:9500541-Sequence Homology, Amino Acid
pubmed:year	1998
pubmed:articleTitle	A mutation in PDS causes non-syndromic recessive deafness.
pubmed:publicationType	Letter, Research Support, U.S. Gov't, P.H.S.