Whole exome sequencing resolves complex phenotype and identifies CC2D2A mutations underlying non-syndromic rod-cone dystrophy
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| Description | scientific article published on 04 November 2018 |
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author: Cécile Méjécase Mélanie Letexier Aline Antonio Fiona Boyard Marine Foussard Isabelle Audo José-Alain Sahel Saddek Mohand-Saïd Said El Shamieh Christina Zeitz |
| Publication date | November 4, 2018 |
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