Investigating the role of ciliary localisation of the TRPP Channel, Polycystin2 (PKD2), on development and progression of polycystic kidney disease
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a common inherited disease, affecting 1:400-1000 people worldwide and leads to end-stage renal failure in most patients before their 6<sup>th</sup> decade. ADPKD is characterised by abnormal persistent cellular proliferation combine...
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University of Oxford
2016
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730208 |