Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2000-11-7
pubmed:abstractText
To analyze the RDH5 gene in patients with fundus albipunctatus with and without cone dystrophy and to determine whether the disease is stationary or progressive and whether the cone dystrophy is a part of fundus albipunctatus or a separate disease.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0146-0404
pubmed:author
pubmed:issnType
Print
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3925-32
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:11053295-Adolescent, pubmed-meshheading:11053295-Adult, pubmed-meshheading:11053295-Aged, pubmed-meshheading:11053295-Alcohol Oxidoreductases, pubmed-meshheading:11053295-Child, pubmed-meshheading:11053295-DNA Mutational Analysis, pubmed-meshheading:11053295-Electroretinography, pubmed-meshheading:11053295-Female, pubmed-meshheading:11053295-Fundus Oculi, pubmed-meshheading:11053295-Humans, pubmed-meshheading:11053295-Male, pubmed-meshheading:11053295-Middle Aged, pubmed-meshheading:11053295-Mutation, pubmed-meshheading:11053295-Night Blindness, pubmed-meshheading:11053295-Ophthalmoscopy, pubmed-meshheading:11053295-Photography, pubmed-meshheading:11053295-Polymerase Chain Reaction, pubmed-meshheading:11053295-Retinal Cone Photoreceptor Cells, pubmed-meshheading:11053295-Retinal Degeneration, pubmed-meshheading:11053295-Visual Acuity
pubmed:year
2000
pubmed:articleTitle
A high association with cone dystrophy in Fundus albipunctatus caused by mutations of the RDH5 gene.
pubmed:affiliation
Department of Ophthalmology, Nagoya University School of Medicine, Nagoya, Japan. makonaka@med.nagoya-u.ac.jp
pubmed:publicationType
Journal Article, Case Reports, Research Support, Non-U.S. Gov't