Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations.

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Cited by papers we hold 2

• RPGR: Its role in photoreceptor physiology, human disease, and future therapies · 2015
  No notice
• Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease · 2013
  No notice

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