No Mutations in the Coding Region of the PRKCG Gene in Three Families with Retinitis Pigmentosa Linked to the RP11 Locus on Chromosome 19q
- 1 September 1999
- journal article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 65 (3), 926-928
- https://doi.org/10.1086/302554
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Segregation of a PRKCG Mutation in Two RP11 FamiliesAmerican Journal of Human Genetics, 1998
- Evidence That the Penetrance of Mutations at the RP11 Locus Causing Dominant Retinitis Pigmentosa Is Influenced by a Gene Linked to the Homologous RP11 AlleleAmerican Journal of Human Genetics, 1997
- Variable Expressivity in a Japanese Family With Autosomal Dominant Retinitis Pigmentosa Closely Linked to Chromosome 19qAmerican Journal of Ophthalmology, 1996
- Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.British Journal of Ophthalmology, 1995
- Dominant Retinitis Pigmentosa With Reduced PenetranceAmerican Journal of Ophthalmology, 1979
- Dominant Retinitis Pigmentosa With Reduced PenetranceAmerican Journal of Ophthalmology, 1969