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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5300
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pubmed:dateCreated |
1997-2-13
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pubmed:databankReference |
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pubmed:abstractText |
Glaucoma is a major cause of blindness and is characterized by progressive degeneration of the optic nerve and is usually associated with elevated intraocular pressure. Analyses of sequence tagged site (STS) content and haplotype sharing between families affected with chromosome 1q-linked open angle glaucoma (GLC1A) were used to prioritize candidate genes for mutation screening. A gene encoding a trabecular meshwork protein (TIGR) mapped to the narrowest disease interval by STS content and radiation hybrid mapping. Thirteen glaucoma patients were found to have one of three mutations in this gene (3.9 percent of the population studied). One of these mutations was also found in a control individual (0.2 percent). Identification of these mutations will aid in early diagnosis, which is essential for optimal application of existing therapies.
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pubmed:grant |
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pubmed:commentsCorrections |
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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 |
Jan
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pubmed:issn |
0036-8075
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pubmed:author |
pubmed-author:AlwardW LWL,
pubmed-author:ClarkA FAF,
pubmed-author:CravenE RER,
pubmed-author:FingertJ HJH,
pubmed-author:KalenakJ WJW,
pubmed-author:MackenD LDL,
pubmed-author:NguyenT DTD,
pubmed-author:NicholsB EBE,
pubmed-author:NishimuraDD,
pubmed-author:NystuenAA,
pubmed-author:PolanskyJ RJR,
pubmed-author:RitchRR,
pubmed-author:SheffieldV CVC,
pubmed-author:StoneE MEM,
pubmed-author:SundenS LSL
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pubmed:issnType |
Print
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pubmed:day |
31
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pubmed:volume |
275
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
668-70
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:9005853-Base Sequence,
pubmed-meshheading:9005853-Chromosome Mapping,
pubmed-meshheading:9005853-Chromosomes, Artificial, Yeast,
pubmed-meshheading:9005853-Chromosomes, Human, Pair 1,
pubmed-meshheading:9005853-Cytoskeletal Proteins,
pubmed-meshheading:9005853-Eye Proteins,
pubmed-meshheading:9005853-Female,
pubmed-meshheading:9005853-Genetic Linkage,
pubmed-meshheading:9005853-Glaucoma, Open-Angle,
pubmed-meshheading:9005853-Glycoproteins,
pubmed-meshheading:9005853-Haplotypes,
pubmed-meshheading:9005853-Humans,
pubmed-meshheading:9005853-Male,
pubmed-meshheading:9005853-Molecular Sequence Data,
pubmed-meshheading:9005853-Mutation,
pubmed-meshheading:9005853-Pedigree,
pubmed-meshheading:9005853-Polymerase Chain Reaction,
pubmed-meshheading:9005853-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:9005853-Sequence Tagged Sites,
pubmed-meshheading:9005853-Trabecular Meshwork
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pubmed:year |
1997
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pubmed:articleTitle |
Identification of a gene that causes primary open angle glaucoma.
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pubmed:affiliation |
Department of Ophthalmology, University of Iowa College of Medicine, Iowa City, IA 52242, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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