Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X-linked retinitis pigmentosa. [electronic resource]
- Human mutation Nov 2002
- 405 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1098-1004
10.1002/humu.9072 doi
Carrier Proteins--genetics Europe Exons Eye Proteins Female Frameshift Mutation Genetic Diseases, X-Linked--genetics Humans Male Mutation Open Reading Frames Polymorphism, Single Nucleotide Retinitis Pigmentosa--genetics