Published 2013
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Dopamine-Serotonin Transporter Disease
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Abstract
Investigators at the Hospital for Sick Children, University of Toronto, Canada report 8 children of a consanguineous Saudi Arabian family who had a similar movement disorder, with autosomal recessive inheritance and a mutation in the SLC18A2 gene that encodes vesicular monoamine transporter 2 [VMAT2].Files
PNB-2013-27-4-1.pdf
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- PNB-2013-27-4-1
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2013When the item was originally created.