Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort
Abstract
PURPOSE. Biallelic variants in CLRN1 are responsible for Usher syndrome 3A and nonsyndromic rod-cone dystrophy (RCD). Retinal findings in Usher syndrome 3A have not been well defined. We report the detailed phenotypic description of RCD associated with CLRN1 variants in a prospective cohort.
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Licence : CC BY - Attribution
Licence : CC BY - Attribution