Volume 17. ADPKD and PFIC1: Diseases with “persistent” or “impaired” raft building

Description

A unified mechanism for any human disease is proposed in this book series based on abnormal membrane microdomain phenotypes. A comparison between Autosomal Dominant Polycystic Kidney Disease (ADPKD), as an example of chronic inflammatory membrane microdomain phenotypes, with Progressive Familial Intrahepatic Cholestasis type 1 (PFIC1), as an example of non-inflammatory membrane microdomain phenotype, is made in this book.