Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa: Molecular vision

Cristina Méndez-Vidal, María González-Del Pozo, Alicia Vela-Boza, Javier Santoyo-López, Francisco J López-Domingo, Carmen Vázquez-Marouschek, Joaquin Dopazo, Salud Borrego, Guillermo Antiñolo

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology