Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2011-5-9
pubmed:abstractText
Mutations in tetraspanin 12 (TSPAN12) have recently been identified as a cause of autosomal dominant familial exudative vitreoretinopathy (FEVR). The purpose of this study was to detect TSPAN12 mutations in Chinese patients with FEVR and to describe the associated phenotypes.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-11029008, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-11076059, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-11409862, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-12172548, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-1307245, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-14507768, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-15024691, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-15223780, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-15346351, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-15981244, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-1642288, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-17093393, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-17325173, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-19324841, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-19837026, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-19837033, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-20159111, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-20159112, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-20340138, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-20354512, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-20688566, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-20938005, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-4058870, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-5394449, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-5571414, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-6626002, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-7362811, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-8252044, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-9056564, http://linkedlifedata.com/resource/pubmed/commentcorrection/21552475-9831343
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1090-0535
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1128-35
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:21552475-Amino Acid Sequence, pubmed-meshheading:21552475-Asian Continental Ancestry Group, pubmed-meshheading:21552475-Base Sequence, pubmed-meshheading:21552475-DNA Mutational Analysis, pubmed-meshheading:21552475-Eye, pubmed-meshheading:21552475-Female, pubmed-meshheading:21552475-Genes, Dominant, pubmed-meshheading:21552475-Genetic Association Studies, pubmed-meshheading:21552475-Genetic Variation, pubmed-meshheading:21552475-Heterozygote, pubmed-meshheading:21552475-Humans, pubmed-meshheading:21552475-Male, pubmed-meshheading:21552475-Membrane Proteins, pubmed-meshheading:21552475-Molecular Sequence Data, pubmed-meshheading:21552475-Mutation, pubmed-meshheading:21552475-Osteoporosis, pubmed-meshheading:21552475-Pedigree, pubmed-meshheading:21552475-Phenotype, pubmed-meshheading:21552475-Tetraspanins, pubmed-meshheading:21552475-Vitreoretinopathy, Proliferative
pubmed:year
2011
pubmed:articleTitle
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes.
pubmed:affiliation
State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, PR China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't