Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2007-7-26
pubmed:abstractText
To identify nucleotide sequence variations in the rhodopsin (RHO) gene of Japanese patients with retinitis pigmentosa (RP) in order to search for mutations or haplotypes responsible for RP.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-10889272, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-10967073, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-10984540, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-11094174, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-12015282, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-1303237, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-1391967, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-15967807, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-1644282, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-16799052, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-1833777, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-1862076, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-1899580, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-2108305, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-2137202, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-2215617, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-6589631, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-6702974, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-7476138, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-7663001, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-7846071, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-7850270, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-7987385, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8076945, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8317502, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8358437, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8473105, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8527802, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8533638, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-8550318, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-9147180, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-9399852, http://linkedlifedata.com/resource/pubmed/commentcorrection/17653048-9888392
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1090-0535
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1038-44
pubmed:dateRevised
2010-9-15
pubmed:meshHeading
pubmed-meshheading:17653048-Asian Continental Ancestry Group, pubmed-meshheading:17653048-Chromosome Mapping, pubmed-meshheading:17653048-DNA Mutational Analysis, pubmed-meshheading:17653048-DNA Transposable Elements, pubmed-meshheading:17653048-Exons, pubmed-meshheading:17653048-Female, pubmed-meshheading:17653048-Gene Deletion, pubmed-meshheading:17653048-Gene Frequency, pubmed-meshheading:17653048-Genetic Variation, pubmed-meshheading:17653048-Haplotypes, pubmed-meshheading:17653048-Humans, pubmed-meshheading:17653048-Introns, pubmed-meshheading:17653048-Linkage Disequilibrium, pubmed-meshheading:17653048-Male, pubmed-meshheading:17653048-Phylogeny, pubmed-meshheading:17653048-Polymorphism, Single Nucleotide, pubmed-meshheading:17653048-Promoter Regions, Genetic, pubmed-meshheading:17653048-Retinitis Pigmentosa, pubmed-meshheading:17653048-Rhodopsin
pubmed:year
2007
pubmed:articleTitle
Mutation screening and haplotype analysis of the rhodopsin gene locus in Japanese patients with retinitis pigmentosa.
pubmed:affiliation
Department of Rehabilitation Engineering, Research Institute, National Rehabilitation Center for Persons with Disabilities, Tokorozawa, Saitama, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't