Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 - 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 Tetreault, Erik G. Puffenberger, James N. Scott, Stéphane Bezieau, André Reis - Dissemin

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Cell Press, American Journal of Human Genetics, 6(97), p. 886-893, 2015

DOI: 10.1016/j.ajhg.2015.11.002

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Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8

Journal article published in 2015 by 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

ORCID

, Martine Tetreault, Erik G. Puffenberger, James N. Scott, Stéphane Bezieau, André Reis

ORCID

and other authors.

This paper is available in a repository.

This paper is available in a repository.

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