Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
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| Description | scientific article published on 28 March 2019 |
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author: Katrina Prescott Aline Antonio Fiona Boyard Christelle Michiels Sabine Defoort-Dhellemmes Marine Foussard Daniel F Schorderet Isabelle Audo Céline Faure Marion Neuillé José-Alain Sahel Markus Preising Dror Sharon Bart Leroy Thomy de Ravel Christina Zeitz |
| Publication date | March 28, 2019 |
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