Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1999-9-7
pubmed:abstractText
To report clinical features and molecular genetic study in three unrelated families in which age-related macular degeneration was observed in grandparents of patients with Stargardt disease.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0002-9394
pubmed:author
pubmed:issnType
Print
pubmed:volume
128
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
173-8
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10458172-ATP-Binding Cassette Transporters, pubmed-meshheading:10458172-Adult, pubmed-meshheading:10458172-Aged, pubmed-meshheading:10458172-Aged, 80 and over, pubmed-meshheading:10458172-Amino Acid Sequence, pubmed-meshheading:10458172-Base Sequence, pubmed-meshheading:10458172-Child, pubmed-meshheading:10458172-DNA, pubmed-meshheading:10458172-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:10458172-Fluorescein Angiography, pubmed-meshheading:10458172-Fundus Oculi, pubmed-meshheading:10458172-Genotype, pubmed-meshheading:10458172-Humans, pubmed-meshheading:10458172-Macular Degeneration, pubmed-meshheading:10458172-Middle Aged, pubmed-meshheading:10458172-Molecular Sequence Data, pubmed-meshheading:10458172-Mutation, Missense, pubmed-meshheading:10458172-Pedigree, pubmed-meshheading:10458172-Phenotype, pubmed-meshheading:10458172-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:10458172-Rod Cell Outer Segment
pubmed:year
1999
pubmed:articleTitle
Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study.
pubmed:affiliation
Clinique Ophtamologique Universitaire de Créteil, France.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't