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
|