Resultados de procura - David Redl

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 por Kym M. Boycott, Chandree L. Beaulieu, Kristin D. Kernohan, Ola H. Gebril, Aziz Mhanni, Albert E. Chudley, David Redl, Wen Qin, Sarah Hampson, Sébastien Küry, Martine Tétreault, Erik G. Puffenberger, James N. Scott, Stéphane Bézieau, André Reis, Steffen Uebe, Johannes Schumacher, Robert A. Hegele, D. Ross McLeod, Marina Gálvez‐Peralta, Jacek Majewski, V. Ramaekers, Daniel W. Nebert, A. Micheil Innes, Jillian S. Parboosingh, Rami Abou Jamra

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