Periventricular heterotopia: broadening of the clinical spectrum of the clathrin 1 gene (CLTC) pathogenic variants D. Martín Fernández-Mayoralas; N. Muñoz Jareño; A. Alba Menéndez; A. Fernández-Jaén;

DYNC1H1 de novo mutation, spinal muscular atrophy and attention problems A.L. Fernández Perrone; P. Moreno Fernández; S. Álvarez; A. Fernández-Jaén;

De novo KAT6B mutation, Say-Barber-Biesecker-Young-Simpson syndrome, and specific language impairment D.M. Fernández-Mayoralas; B. Calleja-Pérez; S. Álvarez; A. Fernández-Jaén;