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Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 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 & Martine Tetreault & Erik G. Puffenberger & James N. Scott & Stéphane Bezieau & André... is a book available to read on EtoBox.

Author
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...
Publisher
The American Society of Human Genetics
Language
EN

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