RP1 and autosomal dominant rodβcone dyst
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Isabelle Audo; Saddek Mohand-SaΓ―d; Claire-Marie Dhaenens; Aurore Germain; Elise
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Article
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2011
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John Wiley and Sons
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English
β 196 KB
Rod-cone dystrophies (retinitis pigmentosa [RP]) are a clinically and genetically heterogeneous group of inherited retinal disorders characterized by photoreceptor degeneration. RP1 is a major gene underlying autosomal dominant (ad) RP, though prevalence figures vary depending on the origin of the c