Oguchi disease: suggestion of linkage to markers on chromosome 2q.

Oguchi disease is a rare autosomal recessive form of congenital stationary night blindness. The condition is associated with fundus discolouration and abnormally slow dark adaptation. Earlier studies suggested that the 48 kD protein S antigen may be involved in the recovery phase of light transducti...

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Bibliografiske detaljer
Main Authors: Maw, M A, John, S, Jablonka, S, Müller, B, Kumaramanickavel, G, Oehlmann, R, Denton, M J, Gal, A
Format: Artigo
Sprog:Inglês
Udgivet: 1995
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050438/
https://ncbi.nlm.nih.gov/pubmed/7616550
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