Mizuo-Nakamura phenomenon (a rare ocular phenomenon)

Oguchi disease, first described in 1907, is a rare autosomal recessive disorder characterized by congenital stationary night blindness with a unique morphological and functional abnormality of the retina. The cause, though largely unknown, is associated with ARRESTIN and RHODOPSIN KINASE gene defect...

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Bibliographic Details
Main Authors: S Agrawal, Shreyansh Doshi, A S Parihar, Nikita Sonawane, Merlin Saldanha
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Journal of Marine Medical Society
Subjects:
Online Access:http://www.marinemedicalsociety.in/article.asp?issn=0975-3605;year=2015;volume=17;issue=1;spage=67;epage=69;aulast=Agrawal;type=0