16170112

Source:http://linkedlifedata.com/resource/pubmed/id/16170112

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0035334, umls-concept:C0035499, umls-concept:C0205314, umls-concept:C0443147, umls-concept:C0679622, umls-concept:C2717879
pubmed:issue	10
pubmed:dateCreated	2005-9-19
pubmed:abstractText	To identify novel or rare rhodopsin gene mutations in patients with autosomal dominant retinitis pigmentosa and description of their clinical phenotype.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-10192380, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-10391212, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-11527955, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-11875049, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-11875050, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-12032732, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-12871954, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-15090652, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-15220479, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-15232620, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1604830, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1634520, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1684223, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1749427, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1765377, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1833777, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1862076, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1924344, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-1987956, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-2021172, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-2137202, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-3344216, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-3873253, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-3977711, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-4294735, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-6450610, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-6975710, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-7981701, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-8025068, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-8045708, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-8406457, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-8541873, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-9602623, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-9618546, http://linkedlifedata.com/resource/pubmed/commentcorrection/16170112-9792858
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0421041
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Rhodopsin
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0007-1161
pubmed:author	pubmed-author:BeschDD, pubmed-author:JägleHH, pubmed-author:JaneckeA RAR, pubmed-author:SchusterAA, pubmed-author:TippmannSS, pubmed-author:WeisschuhNN, pubmed-author:WissingerBB, pubmed-author:ZierlerHH, pubmed-author:ZrennerEE
pubmed:issnType	Print
pubmed:volume	89
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1258-64
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:16170112-Adolescent, pubmed-meshheading:16170112-Adult, pubmed-meshheading:16170112-Age of Onset, pubmed-meshheading:16170112-Amino Acid Sequence, pubmed-meshheading:16170112-Child, pubmed-meshheading:16170112-Child, Preschool, pubmed-meshheading:16170112-DNA Mutational Analysis, pubmed-meshheading:16170112-Female, pubmed-meshheading:16170112-Genes, Dominant, pubmed-meshheading:16170112-Genotype, pubmed-meshheading:16170112-Humans, pubmed-meshheading:16170112-Male, pubmed-meshheading:16170112-Middle Aged, pubmed-meshheading:16170112-Molecular Sequence Data, pubmed-meshheading:16170112-Mutation, pubmed-meshheading:16170112-Mutation, Missense, pubmed-meshheading:16170112-Pedigree, pubmed-meshheading:16170112-Phenotype, pubmed-meshheading:16170112-Polymorphism, Restriction Fragment Length, pubmed-meshheading:16170112-Retinitis Pigmentosa, pubmed-meshheading:16170112-Rhodopsin, pubmed-meshheading:16170112-Visual Acuity, pubmed-meshheading:16170112-Visual Fields
pubmed:year	2005
pubmed:articleTitle	Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa.
pubmed:affiliation	University Eye Hospital, Department of Neuroophthalmology, Schleichstr 12-16, D-72076 Tuebingen, Germany. andreas.schuster@med.uni-tuebingen.de
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't