Retinal Function and Rhodopsin Levels in Autosomal Dominant Retinitis Pigmentosa With Rhodopsin Mutations

Author:

Jacobson Samuel G.,Kemp Colin M.,Sung Ching-Hwa,Nathans Jeremy

Publisher

Elsevier BV

Subject

Ophthalmology

Reference33 articles.

1. Autosomal dominant retinitis pigmentosa (ADRP). Localization of an ADRP gene to the long arm of chromosome 3;McWilliam;Genomics,1989

2. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa;Dryja;Nature,1990

3. Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa;Dryja;N. Engl. J. Med.,1990

4. A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa;Inglehearn;Am. J. Hum. Genet.,1991

5. Sung, C.-H., Davenport, C.M., Hennessey, J.C., Maumenee, I.H., Jacobson, S.G., Heckenlively, J.R., Nowakowski, R., Fishman, G., Gouras, P., and Nathans, J.: Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc. Natl. Acad. Sci. U.S.A. (in press)

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