Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. (Q36369976)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. |
scientific article |
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Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. (English)
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Kym M Boycott
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Chandree L Beaulieu
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A Micheil Innes
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Jillian S Parboosingh
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Albert E Chudley
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Kristin D Kernohan
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Aziz Mhanni
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David Redl
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Wen Qin
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Sarah Hampson
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Sébastien Küry
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Martine Tetreault
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Erik G Puffenberger
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James N Scott
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Stéphane Bezieau
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Steffen Uebe
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Johannes Schumacher
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D Ross McLeod
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Marina Gálvez-Peralta
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Jacek Majewski
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Vincent T Ramaekers
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Care4Rare Canada Consortium
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Daniel W Nebert
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Rami Abou Jamra
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1 December 2015
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886-893
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