A gene therapy approach to Childhood Parkinsonism
Dopamine transporter deficiency syndrome is an inherited primary neurotransmitter disease caused by loss of function mutations in the Dopamine transporter (DAT). DAT is key to dopamine homeostasis and termination of dopamine neurotransmission and recycling. The condition was characterised clinically...
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University College London (University of London)
2017
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| Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.746502 |