Examining CLN7 function in Drosophila
My thesis aims to establish the normal functional role of the transmembrane protein CLN7; mutations in Cln7 cause a debilitating neurodegenerative disorder in infants known as Late Infantile Neuronal Ceroid Lipofuscinosis (LINCL). NCL are a collection of early-onset inherited neurodegenerative disor...
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King's College London (University of London)
2016
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.695769 |