GUCY2D mutations in retinal guanylyl cyclase 1 provide biochemical reasons for dominant cone–rod dystrophy but not for stationary night blindness
Author:
Funder
HHS | NIH | National Eye Institute
Pennsylvania Department of Health
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference67 articles.
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2. Cloning and expression of a second photoreceptor-specific membrane retina guanylyl cyclase (RetGC), RetGC-2;Lowe;Proc. Natl. Acad. Sci. U S A,1995
3. Two membrane forms of guanylyl cyclase found in the eye;Yang;Proc. Natl. Acad. Sci. U.S.A,1995
4. The guanylyl cyclase receptors;Garbers;Methods,1999
5. Disruption of a retinal guanylyl cyclase gene leads to cone-specific dystrophy and paradoxical rod behavior;Yang;J. Neurosci,1999
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