Mutations in the Norrie disease gene: a new mutation in a Japanese family
Br J Ophthalmol
.
1995 Jul;79(7):703-4.
doi: 10.1136/bjo.79.7.703.
Authors
Y Isashiki
,
N Ohba
,
T Yanagita
,
N Hokita
,
Y Hotta
,
M Hayakawa
,
K Fujiki
,
U Tanabe
PMID:
7662640
PMCID:
PMC505203
DOI:
10.1136/bjo.79.7.703
No abstract available
Publication types
Case Reports
Letter
Research Support, Non-U.S. Gov't
MeSH terms
Adolescent
Blindness / genetics*
Genetic Linkage
Humans
Male
Pedigree
Point Mutation*
X Chromosome