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...
Main Author: | |
---|---|
Published: |
Cardiff University
2006
|
Subjects: | |
Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.583756 |