Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2003-4-25
pubmed:abstractText
Mutations in the systemically expressed pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 have recently been associated with autosomal dominant retinitis pigmentosa (adRP). This study was intended to identify mutations in PRPF3, PRPF8, and PRPF31 in 150 Spanish families affected by adRP, to measure the contribution of mutations in these genes to adRP in that population, and to correlate RP phenotype expression with mutations in pre-mRNA splicing-factor genes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0146-0404
pubmed:author
pubmed:issnType
Print
pubmed:volume
44
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2171-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12714658-Adolescent, pubmed-meshheading:12714658-Adult, pubmed-meshheading:12714658-Aged, pubmed-meshheading:12714658-Alleles, pubmed-meshheading:12714658-Carrier Proteins, pubmed-meshheading:12714658-DNA Mutational Analysis, pubmed-meshheading:12714658-Electrooculography, pubmed-meshheading:12714658-Electroretinography, pubmed-meshheading:12714658-Eye Proteins, pubmed-meshheading:12714658-Female, pubmed-meshheading:12714658-Genes, Dominant, pubmed-meshheading:12714658-Humans, pubmed-meshheading:12714658-Male, pubmed-meshheading:12714658-Middle Aged, pubmed-meshheading:12714658-Mutation, pubmed-meshheading:12714658-Nuclear Proteins, pubmed-meshheading:12714658-Pedigree, pubmed-meshheading:12714658-Polymerase Chain Reaction, pubmed-meshheading:12714658-RNA Precursors, pubmed-meshheading:12714658-RNA Splicing, pubmed-meshheading:12714658-Retinitis Pigmentosa, pubmed-meshheading:12714658-Ribonucleoprotein, U4-U6 Small Nuclear, pubmed-meshheading:12714658-Sequence Analysis, DNA, pubmed-meshheading:12714658-Spain
pubmed:year
2003
pubmed:articleTitle
Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa.
pubmed:affiliation
Laboratory of Biology and Molecular Genetics, Laboratory of Service, Consorci Sanitari de Terrassa, Hospital de Terrassa, Terrassa, Spain.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't