Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8
Kym M. Boycott(University of Ottawa), Chandree L. Beaulieu(University of Ottawa), Kristin D. Kernohan(University of Ottawa), Ola H. Gebril(National Research Centre), Aziz Mhanni(University of Manitoba), Albert E. Chudley(University of Manitoba), David Redl(University of Calgary), Wen Qin(University of Ottawa), Sarah Hampson(University of Ottawa), Sébastien Küry, Martine Tétreault(McGill University), Erik G. Puffenberger(Clinic for Special Children), James N. Scott(Foothills Medical Centre), Stéphane Bezieau, André Reis(Friedrich-Alexander-Universität Erlangen-Nürnberg), Steffen Uebe(Friedrich-Alexander-Universität Erlangen-Nürnberg), Johannes Schumacher(University of Bonn), Robert A. Hegele(Western University), D. Ross McLeod(University of Calgary), Marina Gálvez‐Peralta(University of Cincinnati Medical Center), Jacek Majewski(McGill University), V. Ramaekers(Centre Hospitalier Universitaire de Liège), Daniel W. Nebert(Cincinnati Children's Hospital Medical Center), A. Micheil Innes(University of Calgary), Jillian S. Parboosingh(University of Calgary), Rami Abou Jamra(Friedrich-Alexander-Universität Erlangen-Nürnberg)
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