Comprehensive survey of mutations in RP2
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ValΓ©rie Pelletier; Marguerite Jambou; Nathalie Delphin; Elena Zinovieva; Morgane
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Article
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2006
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John Wiley and Sons
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English
β 447 KB
Communicated by Daniel F. Schorderet X-linked forms of retinitis pigmentosa (RP) (XLRP) account for 10 to 20% of families with RP and are mainly accounted for by mutations in the RP2 or RP GTPase regulator (RPGR) genes. We report the screening of these genes in a cohort of 127 French family comprisi