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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
1997-5-23
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pubmed:abstractText |
Retinopathy of prematurity (ROP) is a retinal vascular disease occurring in infants with short gestational age and low birth weight and can lead to retinal detachment (ROP stages 4 and 5). X-linked familial exudative vitreoretinopathy is phenotypically similar to ROP and has been associated with mutations in the Norrie disease (ND) gene in some cases.
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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 |
May
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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 |
115
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
651-5
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:9152134-DNA Mutational Analysis,
pubmed-meshheading:9152134-DNA Primers,
pubmed-meshheading:9152134-Deafness,
pubmed-meshheading:9152134-Electrophoresis, Agar Gel,
pubmed-meshheading:9152134-Eye Proteins,
pubmed-meshheading:9152134-Female,
pubmed-meshheading:9152134-Humans,
pubmed-meshheading:9152134-Infant, Newborn,
pubmed-meshheading:9152134-Intellectual Disability,
pubmed-meshheading:9152134-Male,
pubmed-meshheading:9152134-Mutation,
pubmed-meshheading:9152134-Nerve Tissue Proteins,
pubmed-meshheading:9152134-Pedigree,
pubmed-meshheading:9152134-Polymerase Chain Reaction,
pubmed-meshheading:9152134-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:9152134-Retinal Diseases,
pubmed-meshheading:9152134-Retinopathy of Prematurity
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pubmed:year |
1997
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pubmed:articleTitle |
Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity.
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pubmed:affiliation |
Eye Research Institute, Oakland University, Rochester, Mich, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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