Genetic Factors Modifying Clinical Expression of Autosomal Dominant RP
- 31 December 2005
- book chapter
- Published by Springer Nature
- Vol. 572, 3-8
- https://doi.org/10.1007/0-387-32442-9_1
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors.2002
- Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).2001
- Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesHuman Mutation, 2000
- Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa.2000
- Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaHuman Molecular Genetics, 1999
- A Nonsense Mutation in a Novel Gene Is Associated With Retinitis Pigmentosa in a Family Linked to the RP1 LocusHuman Molecular Genetics, 1999
- Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosaNature Genetics, 1999
- Multipoint Oligogenic Analysis of Age-at-Onset Data with Applications to Alzheimer Disease PedigreesAmerican Journal of Human Genetics, 1999
- Monte carlo markov chain methods for genome screeningGenetic Epidemiology, 1999
- 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