Retinal guanylate cyclase gene

Downes, S.M., Payne, A.M., Kelsell, R.E., Fitzke, F.W., Holder, G.E., Hunt, D.M., Moore, A.T., and Bird, A.C. (2001b). Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1. Arch. Ophthalmol. 119 1667-1673. 

El-Shanti, H., Al-Salem, M., El-Najjar, M., Ajlouni, K., Beck, J., Sheffiled, V.C., and Stone, E.M. (1999). A nonsense mutation in the retinal specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred kindred from Jordan. J. Med. Genet. 36 862-865. 

Semp 1 e-Rowland, S.L., Lee, N.R., Van Hooser, J.P., Palczewski, K., and Baehr, W. (1998). A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype. Proc. Natl. Acad. Sci. USA 95 1271—1276. 

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