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Literature DB >> 10581022

Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.

H Morimura, F Saindelle-Ribeaudeau, E L Berson, T P Dryja.

Abstract

Entities: Chemical Disease Gene Mutation Species

Mesh：

Substances：

Year: 1999 PMID： 10581022 DOI： 10.1038/70496

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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47 in total

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4. Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina.

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7. Photic generation of 11-cis-retinal in bovine retinal pigment epithelium.

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