Publications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (2)

2021

  1. CPEB alteration and aberrant transcriptome-polyadenylation lead to a treatable SLC19A3 deficiency in Huntington’s disease

    Science Translational Medicine, Vol. 13, Núm. 613

2018

  1. Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing

    Nature, Vol. 560, Núm. 7719, pp. 441-446