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...
Bewaard in:
| Hoofdauteur: | |
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| Formaat: | Boek |
| Gepubliceerd in: |
Pediatric Neurology Briefs Publishers,
2013-04-01T00:00:00Z.
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Internet
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| Plaatsingsnummer: |
A1234.567 |
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| Kopie 1 | Beschikbaar |