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- 2020
-
Mark
Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants
(
- Contribution to journal › Article
- 2019
-
Mark
Long-term follow-up of retinal function and structure in trpm1-associated complete congenital stationary night blindness
(
- Contribution to journal › Article
- 2018
-
Mark
Congenital stationary night blindness associated with morning glory disc malformation : a novel hemizygous mutation in CACNA1F
(
- Contribution to journal › Letter
- 2017
-
Mark
Heterozygous mutation in OTX2 associated with early-onset retinal dystrophy with atypical maculopathy
(
- Contribution to journal › Article