Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit

por Ariani, F, Mari, F, Amitrano, S, Di Marco, C, Artuso, R, Scala, E, Meloni, I, Della Volpe, R, Rossi, A, Bokhoven, H, Renieri, A
Publicado 2013