Associated Papers
Retinal Phenotype of Patients with CLRN1-Associated Usher 3A Syndrome in French Light4Deaf Cohort.
Smirnov VM et al.
Investigative Ophthalmology & Visual Science, 2022
Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.
Ratnam K et al.
Jama Ophthalmology, 2013
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