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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
1994-7-12
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pubmed:abstractText |
We identified a large family affected with a macular dystrophy whose main clinical features are similar to those of Stargardt's disease. Unlike true Stargardt's disease, the disorder in this family is inherited in an autosomal dominant fashion. We sought to identify the chromosomal location of the disease-causing gene and to clinically define the phenotype in a number of affected family members.
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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 |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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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 |
112
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
765-72
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:8002834-Adolescent,
pubmed-meshheading:8002834-Adult,
pubmed-meshheading:8002834-Aged,
pubmed-meshheading:8002834-Aged, 80 and over,
pubmed-meshheading:8002834-Child,
pubmed-meshheading:8002834-Child, Preschool,
pubmed-meshheading:8002834-Chromosomes, Human, Pair 6,
pubmed-meshheading:8002834-Electroretinography,
pubmed-meshheading:8002834-Female,
pubmed-meshheading:8002834-Genetic Linkage,
pubmed-meshheading:8002834-Humans,
pubmed-meshheading:8002834-Macular Degeneration,
pubmed-meshheading:8002834-Male,
pubmed-meshheading:8002834-Middle Aged,
pubmed-meshheading:8002834-Pedigree,
pubmed-meshheading:8002834-Retina,
pubmed-meshheading:8002834-Visual Fields
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pubmed:year |
1994
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pubmed:articleTitle |
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.
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pubmed:affiliation |
Department of Ophthalmology, University of Iowa College of Medicine, Iowa City.
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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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