Molecular analysis of a Tsc1-deficient mouse

Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutation in either the TSC1 or TSC2 genes and characterised by the development of benign hamartomatous growths in multiple organ systems. We have inactivated Tsd in the mouse germ line by gene targeting in ES cells and conf...

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Bibliographic Details
Main Author: Wilson, Catherine
Published: Cardiff University 2006
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.583756