Novel 2336-2337delCT mutation in RP1 gene in a japanese family with autosomal dominant retinitis pigmentosa
- 30 June 2004
- journal article
- research article
- Published by Elsevier BV in American Journal of Ophthalmology
- Vol. 137 (6), 1137-1139
- https://doi.org/10.1016/j.ajo.2003.12.037
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- RP1 in Chinese: Eight novel variants and evidence that truncation of the extreme C-terminal does not cause retinitis pigmentosaHuman Mutation, 2001
- Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaHuman Molecular Genetics, 1999
- Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosaNature Genetics, 1999
- Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.Nature Genetics, 1999