Condition: OGUCHI DISEASE 2
rs570621429 in
GRK1 gene and
OGUCHI DISEASE 2
PMID 17070587 2007 A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.
PMID 9020843 1997 Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.