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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2009-3-26
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pubmed:abstractText |
Primary open-angle glaucoma (POAG) is a common disease requiring early diagnosis and treatment to avoid asymptomatic visual field loss and eventual blindness. LMX1B mutations cause dominantly-inherited Nail-Patella syndrome in which approximately 33% of patients develop glaucoma. This study investigated the wider role of LMX1B in POAG.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1552-5783
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
50
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1522-30
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:18952915-Aged,
pubmed-meshheading:18952915-Case-Control Studies,
pubmed-meshheading:18952915-Female,
pubmed-meshheading:18952915-Genetic Predisposition to Disease,
pubmed-meshheading:18952915-Glaucoma, Open-Angle,
pubmed-meshheading:18952915-Haplotypes,
pubmed-meshheading:18952915-Homeodomain Proteins,
pubmed-meshheading:18952915-Humans,
pubmed-meshheading:18952915-Intraocular Pressure,
pubmed-meshheading:18952915-LIM-Homeodomain Proteins,
pubmed-meshheading:18952915-Male,
pubmed-meshheading:18952915-Ocular Hypertension,
pubmed-meshheading:18952915-Polymorphism, Single Nucleotide,
pubmed-meshheading:18952915-Risk Factors,
pubmed-meshheading:18952915-Transcription Factors
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pubmed:year |
2009
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pubmed:articleTitle |
Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes.
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pubmed:affiliation |
Developmental Biology Unit, University College London Institute of Child Health and Great Ormond Street Hospital for Children NHS Trust, London, United Kingdom.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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