Oguchi disease with sectoral retinitis pigmentosa harboring adenine deletion at position 1147 in the arrestin gene
- 1 February 1998
- journal article
- case report
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 125 (2) , 249-251
- https://doi.org/10.1016/s0002-9394(99)80100-7
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindnessNature Genetics, 1997
- A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in JapaneseNature Genetics, 1995
- Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/ RDS and ROM1 LociScience, 1994