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15491396
Source:
http://linkedlifedata.com/resource/pubmed/id/15491396
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51
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0015576
,
umls-concept:C0265234
,
umls-concept:C0544885
,
umls-concept:C1414490
,
umls-concept:C1556094
pubmed:issue
5
pubmed:dateCreated
2004-10-19
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/100886002
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Codon, Nonsense
,
http://linkedlifedata.com/resource/pubmed/chemical/EYA1 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides...
,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases
,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1328-8067
pubmed:author
pubmed-author:KurotakiToshiakiT
,
pubmed-author:SawadaMasakoM
,
pubmed-author:ShinomiyaNoriakiN
,
pubmed-author:UnoTakuT
pubmed:issnType
Print
pubmed:volume
46
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
615-7
pubmed:dateRevised
2008-5-21
pubmed:meshHeading
pubmed-meshheading:15491396-Base Sequence
,
pubmed-meshheading:15491396-Branchio-Oto-Renal Syndrome
,
pubmed-meshheading:15491396-Codon, Nonsense
,
pubmed-meshheading:15491396-DNA Mutational Analysis
,
pubmed-meshheading:15491396-Female
,
pubmed-meshheading:15491396-Humans
,
pubmed-meshheading:15491396-Intracellular Signaling Peptides and Proteins
,
pubmed-meshheading:15491396-Japan
,
pubmed-meshheading:15491396-Kidney
,
pubmed-meshheading:15491396-Magnetic Resonance Imaging
,
pubmed-meshheading:15491396-Male
,
pubmed-meshheading:15491396-Nuclear Proteins
,
pubmed-meshheading:15491396-Pedigree
,
pubmed-meshheading:15491396-Protein Tyrosine Phosphatases
,
pubmed-meshheading:15491396-Trans-Activators
pubmed:year
2004
pubmed:articleTitle
EYA1 gene nonsense mutation in a Japanese family with branchio-oto-renal syndrome.
pubmed:affiliation
Second Department of Pediatrics, Toho University School of Medicine, Toho, Japan.
pubmed:publicationType
Journal Article
,
Case Reports
,
Research Support, Non-U.S. Gov't