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- 2018
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Mark
Novel causative variants in patients with achromatopsia
(
- Contribution to journal › Article
- 2017
-
Mark
The clinical phenotype of CNGA3-related achromatopsia : Pretreatment characterization in preparation of a gene replacement therapy trial
(
- Contribution to journal › Article
- 2005
-
Mark
CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia
(
- Contribution to journal › Article