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Whole-exome sequencing allows the identification of new causal mutations and candidate genes in unsolved inherited retinal dystrophy patients

Marta Martin-Sanchez,Elena Fernandez-Suarez,Nereida Bravo-Gil,Cristina Mendez-Vidal,Maria Gonzalez-del Pozo,Marcela Mena,Jose Manuel Mejias-Carrasco,Alejandro Garcia-Nunez,Enrique Rodriguez-de la Rua,Maria Jose Morillo Sanchez,Salud Borrego,Guillermo Antinolo

EUROPEAN JOURNAL OF HUMAN GENETICS（2024）

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