Dopamine-Serotonin Transporter Disease
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...
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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2013-04-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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]. |
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| Item Description: | 1043-3155 2166-6482 10.15844/pedneurbriefs-27-4-1 |