The purpose of this study was to perform a detailed longitudinal phenotyping of X-linked retinitis pigmentosa (RP) caused by mutations in the RPGR gene during a long follow-up period.
Spectrum of Disease Severity in Patients With X-Linked Retinitis Pigmentosa Due to RPGR Mutations
Di Iorio, Valentina;Karali, Marianthi;Melillo, Paolo;Testa, Francesco
;Brunetti-Pierri, Raffaella;Banfi, Sandro
;Simonelli, Francesca
2020
Abstract
The purpose of this study was to perform a detailed longitudinal phenotyping of X-linked retinitis pigmentosa (RP) caused by mutations in the RPGR gene during a long follow-up period.File in questo prodotto:
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