Publications in collaboration with researchers from Centro de Investigación Biomédica en Red sobre Enfermedades Raras (1)

2020

  1. CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix

    Human Genetics, Vol. 139, Núm. 10, pp. 1209-1231