17653038

Source:http://linkedlifedata.com/resource/pubmed/id/17653038

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010036, umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1258464, umls-concept:C1273518, umls-concept:C1416715, umls-concept:C1836408
pubmed:dateCreated	2007-7-26
pubmed:abstractText	To determine if a mutation within the coding region of the keratin 12 gene (KRT12) is responsible for a severe form of Meesmann's corneal dystrophy.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/EY10608, http://linkedlifedata.com/resource/pubmed/grant/K08 EY00350
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-10612503, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-10644419, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-10781519, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-12084738, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-12543196, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-1372711, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-1381287, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-15148206, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-16227835, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-16352477, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-1691189, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-1707331, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-1717157, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-1720261, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-2440750, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-301357, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-6979375, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-7506606, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-8977471, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-9171831, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653038-9399908
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9605351
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Arginine, http://linkedlifedata.com/resource/pubmed/chemical/Keratin-12, http://linkedlifedata.com/resource/pubmed/chemical/Proline
pubmed:status	MEDLINE
pubmed:issn	1090-0535
pubmed:author	pubmed-author:BaylinEric BEB, pubmed-author:ClinchThomas ETE, pubmed-author:DaigerStephen PSP, pubmed-author:FontRamonR, pubmed-author:NakamuraHisashiH, pubmed-author:PeposeJay SJS, pubmed-author:SullivanLori SLS, pubmed-author:YeeRichard WRW, pubmed-author:ZhaoXinping CXC
pubmed:issnType	Electronic
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	975-80
pubmed:dateRevised	2010-9-14
pubmed:meshHeading	pubmed-meshheading:17653038-Adult, pubmed-meshheading:17653038-Amino Acid Motifs, pubmed-meshheading:17653038-Arginine, pubmed-meshheading:17653038-Corneal Dystrophy, Juvenile Epithelial of Meesmann, pubmed-meshheading:17653038-Epithelium, Corneal, pubmed-meshheading:17653038-Exons, pubmed-meshheading:17653038-Genes, Dominant, pubmed-meshheading:17653038-Heterozygote, pubmed-meshheading:17653038-Humans, pubmed-meshheading:17653038-Keratin-12, pubmed-meshheading:17653038-Male, pubmed-meshheading:17653038-Microscopy, Electron, pubmed-meshheading:17653038-Molecular Biology, pubmed-meshheading:17653038-Mutation, Missense, pubmed-meshheading:17653038-Pedigree, pubmed-meshheading:17653038-Phenotype, pubmed-meshheading:17653038-Proline, pubmed-meshheading:17653038-Severity of Illness Index
pubmed:year	2007
pubmed:articleTitle	A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.
pubmed:affiliation	School of Public Health, The University of Texas Health Science Center at Houston, Houston, Texas 77030, USA.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural