Dopamine-Serotonin Transporter Disease
DOI:
https://doi.org/10.15844/pedneurbriefs-27-4-1Keywords:
Norepinephrine, Neurologic Examination, Dopamine AgonistsAbstract
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].Published
2013-04-01
Issue
Section
Movement Disorders
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