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
Myopia with X-linked retinitis pigmentosa results from a novel gross deletion of RPGR gene.
Li HP et al.
International Journal of Ophthalmology, 2020
CLINICAL AND GENETIC CHARACTERISTICS OF MALE PATIENTS WITH RPGR-ASSOCIATED RETINAL DYSTROPHIES: A Long-Term Follow-up Study.
Talib M et al.
Retina (philadelphia, Pa.), 2019
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