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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2015-01-01
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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 |