|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
1998-7-20
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|
pubmed:abstractText |
Lattice corneal dystrophy type I is one of the frequent forms of stromal dystrophies following autosomal dominant inheritance. The beta-IG-h3 gene encoding keratoepithelin on the long arm of chromosome 5 has recently been described as disease gene for lattice corneal dystrophy type I as well as for three other corneal dystrophies with autosomal dominant pattern of inheritance.
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|
pubmed:language |
ger
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0023-2165
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
212
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
154-8
|
|
pubmed:dateRevised |
2009-11-11
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|
pubmed:meshHeading |
pubmed-meshheading:9592740-Adult,
pubmed-meshheading:9592740-Aged,
pubmed-meshheading:9592740-Chromosome Aberrations,
pubmed-meshheading:9592740-Chromosome Disorders,
pubmed-meshheading:9592740-Chromosomes, Human, Pair 5,
pubmed-meshheading:9592740-Corneal Dystrophies, Hereditary,
pubmed-meshheading:9592740-DNA, Complementary,
pubmed-meshheading:9592740-DNA Mutational Analysis,
pubmed-meshheading:9592740-Extracellular Matrix Proteins,
pubmed-meshheading:9592740-Eye Proteins,
pubmed-meshheading:9592740-Female,
pubmed-meshheading:9592740-Genes, Dominant,
pubmed-meshheading:9592740-Heterozygote Detection,
pubmed-meshheading:9592740-Humans,
pubmed-meshheading:9592740-Male,
pubmed-meshheading:9592740-Middle Aged,
pubmed-meshheading:9592740-Pedigree,
pubmed-meshheading:9592740-Polymerase Chain Reaction,
pubmed-meshheading:9592740-RNA, Messenger
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|
pubmed:year |
1998
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|
pubmed:articleTitle |
[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family].
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|
pubmed:affiliation |
Institut für Humangenetik, Universitäts-Krankenhaus Eppendorf, Hamburg.
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|
pubmed:publicationType |
Journal Article,
English Abstract
|
