Publicacións nas que colabora con Marta Cortón Pérez (3)

2016

  1. Identification of the photoreceptor transcriptional Co-Repressor SAMD11 as novel cause of autosomal recessive retinitis pigmentosa

    Scientific Reports, Vol. 6

2015

  1. Human iPSC derived disease model of MERTK-associated retinitis pigmentosa

    Scientific Reports, Vol. 5

  2. Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations

    Human Molecular Genetics, Vol. 24, Núm. 14, pp. 4037-4048