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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
1993-12-7
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pubmed:abstractText |
To ascertain and characterize rhodopsin gene mutations in autosomal dominant retinitis pigmentosa and to correlate these mutations with the clinical phenotypes.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0003-9950
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
111
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1512-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8240107-Adult,
pubmed-meshheading:8240107-Aged,
pubmed-meshheading:8240107-Base Sequence,
pubmed-meshheading:8240107-Chromosome Aberrations,
pubmed-meshheading:8240107-Chromosome Disorders,
pubmed-meshheading:8240107-Chromosomes, Human, Pair 3,
pubmed-meshheading:8240107-Codon,
pubmed-meshheading:8240107-DNA Primers,
pubmed-meshheading:8240107-Electroretinography,
pubmed-meshheading:8240107-Female,
pubmed-meshheading:8240107-Fundus Oculi,
pubmed-meshheading:8240107-Humans,
pubmed-meshheading:8240107-Male,
pubmed-meshheading:8240107-Middle Aged,
pubmed-meshheading:8240107-Molecular Sequence Data,
pubmed-meshheading:8240107-Mutation,
pubmed-meshheading:8240107-Pedigree,
pubmed-meshheading:8240107-Phenotype,
pubmed-meshheading:8240107-Retinitis Pigmentosa,
pubmed-meshheading:8240107-Rhodopsin,
pubmed-meshheading:8240107-Visual Fields
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pubmed:year |
1993
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pubmed:articleTitle |
A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease.
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pubmed:affiliation |
Department of Ophthalmology, University of Melbourne, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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