Article
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.
Journal of medical genetics - 1 Nov 1994
Aldred M A, Teague P W, Jay M, Bundey S, Redmond R M, Jay B, Bird A C, Bhattacharya S S, Wright A F
Abstract excerpt
Three families with retinitis pigmentosa (RP) are described in which the disorder shows apparent X linked inheritance but does not show linkage to the RP2 and RP3 regions of the short arm of the X chromosome. The families are also inconsistent with a localisation of the disease gene between DXS16...
Topics
- Adult
- Alleles
- Chromosome Mapping
- DNA
- Female
- Genetic Linkage
- Haplotypes
- Humans
- Male
- Pedigree
- Retinitis Pigmentosa
- X Chromosome
