Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders

por González-Morón, D., Vishnopolska, S., Consalvo, D., Medina, N., Marti, M., Córdoba, M., Vazquez-Dusefante, C., Claverie, S., Rodríguez-Quiroga, S.A., Vega, P., Silva, W., Kochen, S., Kauffman, M.A.

Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder

por Nemirovsky, S.I., Córdoba, M., Zaiat, J.J., Completa, S.P., Vega, P.A., González-Morón, D., Medina, N.M., Fabbro, M., Romero, S., Brun, B., Revale, S., Ogara, M.F., Pecci, A., Marti, M., Vazquez, M., Turjanski, A., Kauffman, M.A.