Associated Papers
Genotype-Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review.
Yang J et al.
Frontiers in Genetics, 2021
34745198 (PubMed )
Supplement: Table_1.XLSX › Sheet1
Next-generation sequencing identifies unexpected genotype-phenotype correlations in patients with retinitis pigmentosa.
Birtel J et al.
Plos One, 2018
RPGR: Its role in photoreceptor physiology, human disease, and future therapies.
Megaw RD et al.
Experimental Eye Research, 2015
RPGR and RP2: targets for the treatment of X-linked retinitis pigmentosa?
Veltel S et al.
Expert Opinion on Therapeutic Targets, 2009
Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype-phenotype correlations and impact on genetic counseling.
Pelletier V et al.
Human Mutation, 2007
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