Study of MeCP2 function in a mouse model of Rett syndrome
It is now commonly agreed that Rett Syndrome is a monogenic neurological disease caused by mutations in <i>MECP2 </i>gene. Rett Syndrome mainly occurs in girls and it is characterised by a period of normal development until around 618 months, followed by a rapid regression. After the re...
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University of Edinburgh
2005
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.653565 |