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- 2020
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Mark
Clinical phenotype and course of PDE6A-associated retinitis pigmentosa disease, characterized in preparation for a gene supplementation trial
(
- Contribution to journal › Article
- 2018
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Mark
Combination of cGMP analogue and drug delivery system provides functional protection in hereditary retinal degeneration
2018) In Proceedings of the National Academy of Sciences of the United States of America 115(13). p.2997-3006(
- Contribution to journal › Article
- 2016
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Mark
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects
(
- Contribution to journal › Article
- 2014
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Mark
Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration.
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- Contribution to journal › Article
- 2013
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Mark
Phenotypic map of porcine retinal ganglion cells
(
- Contribution to journal › Article