Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31.
Deery EC; Vithana EN; Newbold RJ; Gallon VA; Bhattacharya SS; Warren MJ; Hunt DM; Wilkie SE; Human Molecular Genetics, 2002, vol. 11, issue 25, p 3209, ISSN 09646906. ISBN 09646906.

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