https://www.selleckchem.com/pr....oducts/ac-fltd-cmk.h
Oguchi disease is a rare autosomal recessive form of congenital stationary night blindness (CSN characterized by specific features such as golden-brown discoloration of the fundus called Mizuo-Nakamura phenomenon which is distinguishable by fundoscopy, and retinography. Clinical diagnosis is confirmed through genetic test. Two known genes in pathogenesis of Oguchi disease are SAG and GRK1. A 35-year-old Iranian male exhibiting the clinical features of congenital stationary night blindness, was referred to the genetic clinic of Dr.

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https://riddle-christie.though....tlanes.net/10-media-
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