Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation

por Issa, Lina, Mueller, Katrin, Seufert, Katja, Kraemer, Nadine, Rosenkotter, Henning, Ninnemann, Olaf, Buob, Michael, Kaindl, Angela M, Morris-Rosendahl, Deborah J
Publicado 2013