Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.
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| Description | scientific article |
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author: Ola H Gebril Robert A. Hegele A. Micheil Innes André Reis Albert E Chudley Chandree L Beaulieu Jillian S Parboosingh Kym M Boycott Sébastien Küry |
| Publication date | December 1, 2015 |
| Language | English |
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