Méndez-Vidal, C., Bravo-Gil, N., González del Pozo, M., Vela-Boza, A., Dopazo, J., Borrego, S., & Antiñolo Gil, G. (2014). Novel RP1 mutations and a recurrent BBS1 variant explain the co-existence of two distinct retinal phenotypes in the same pedigree.

Méndez-Vidal, Cristina, Nereida Bravo-Gil, María González del Pozo, Alicia Vela-Boza, Joaquín Dopazo, Salud Borrego, y Guillermo Antiñolo Gil. Novel RP1 Mutations and a Recurrent BBS1 Variant Explain the Co-existence of Two Distinct Retinal Phenotypes in the Same Pedigree. 2014.

Méndez-Vidal, Cristina, et al. Novel RP1 Mutations and a Recurrent BBS1 Variant Explain the Co-existence of Two Distinct Retinal Phenotypes in the Same Pedigree. 2014.