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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| Natura: | Artigo |
| Lingua: | Inglês |
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Pediatric Neurology Briefs Publishers
2013-04-01
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| Serie: | Pediatric Neurology Briefs |
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| Accesso online: | https://www.pediatricneurologybriefs.com/articles/430 |
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