Source:http://linkedlifedata.com/resource/pubmed/id/11151217
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2001-1-26
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pubmed:abstractText |
Retinitis pigmentosa (RP) is the most prevalent inherited degeneration in the retina. The clinical manifestations are variable in terms of severity, age of onset and progression. The clinical variation is paralleled by genetic heterogeneity (more than 20 different loci have been described to date). The aim of this work was to identify mutations in rhodopsin gene and to determine the frequencies of the different genetic forms of RP in the Galician population.
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pubmed:language |
spa
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0365-6691
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
75
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
547-53
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11151217-Adolescent,
pubmed-meshheading:11151217-Adult,
pubmed-meshheading:11151217-Aged,
pubmed-meshheading:11151217-Child,
pubmed-meshheading:11151217-Female,
pubmed-meshheading:11151217-Humans,
pubmed-meshheading:11151217-Male,
pubmed-meshheading:11151217-Middle Aged,
pubmed-meshheading:11151217-Point Mutation,
pubmed-meshheading:11151217-Retinitis Pigmentosa,
pubmed-meshheading:11151217-Rhodopsin,
pubmed-meshheading:11151217-Spain
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pubmed:year |
2000
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pubmed:articleTitle |
[Retinitis pigmentosa: results of rhodopsin gene analysis in the Galician population].
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pubmed:affiliation |
Servicio de Oftalmología, Instituto Gallego de Oftalmología, Instituto de Medicina Legal, Universidad de Santiago de Compostela, España.
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pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
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