Autosomal dominant retinal dystrophy (Rdy) in Abyssinian cats: exclusion of PDE6G and ROM1 and likely exclusion of Rhodopsin as candidate genes
Author:
Publisher
Wiley
Subject
Genetics,Animal Science and Zoology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2052.2002.00914.x/fullpdf
Reference25 articles.
1. Rhodopsin mutations in autosomal dominant retinitis pigmentosa;Al-Maghtheh;Human Mutation,1993
2. Autosomal dominant progressive retinal atrophy in Abyssinian cats;Barnett;Journal of Heredity,1985
3. Polymorphisms and rare sequence variants at the ROM-1 locus;Bascom;Human Molecular Genetics,1993
4. A mutation in NRL is associated with autosomal dominant retinitis pigmentosa;Bessant;Nature Genetics,1999
5. Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa;Chakarova;Human Molecular Genetics,2002
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