7 results on '"Kim, Angela H."'
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2. Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa
3. Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
4. A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
5. Congenital Stationary Night Blindness: Clinical and Genetic Features
6. Chorioretinal atrophy following voretigene neparvovec despite the presence of fundus autofluorescence
7. Neurological toxicities associated with chimeric antigen receptor T-cell therapy
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