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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 |
2009-4-16
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pubmed:abstractText |
To investigate the possibility of collagen type VIII alpha2 (COL8A2) as a potential susceptibility gene for Korean patients with Fuchs' corneal dystrophy (FECD), we performed mutation screening of the COL8A2 gene.
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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 |
1476-5454
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
895-903
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pubmed:meshHeading |
pubmed-meshheading:18464802-Adult,
pubmed-meshheading:18464802-Aged,
pubmed-meshheading:18464802-Aged, 80 and over,
pubmed-meshheading:18464802-Alleles,
pubmed-meshheading:18464802-Amino Acid Substitution,
pubmed-meshheading:18464802-Asian Continental Ancestry Group,
pubmed-meshheading:18464802-Collagen Type VIII,
pubmed-meshheading:18464802-DNA Mutational Analysis,
pubmed-meshheading:18464802-Exons,
pubmed-meshheading:18464802-Female,
pubmed-meshheading:18464802-Fuchs' Endothelial Dystrophy,
pubmed-meshheading:18464802-Gene Frequency,
pubmed-meshheading:18464802-Humans,
pubmed-meshheading:18464802-Korea,
pubmed-meshheading:18464802-Male,
pubmed-meshheading:18464802-Middle Aged,
pubmed-meshheading:18464802-Mutation,
pubmed-meshheading:18464802-Pedigree,
pubmed-meshheading:18464802-Polymerase Chain Reaction,
pubmed-meshheading:18464802-Young Adult
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pubmed:year |
2009
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pubmed:articleTitle |
Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients.
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pubmed:affiliation |
Laboratory of Ophthalmology and Visual Science, The Catholic University of Korea, Seoul, Republic of Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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