20/12/2016
New publication from PCF:
http://www.sciencedirect.com/science/article/pii/S246802491630170X
Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in the fibrinogen A alpha chain (FGA) gene, and it is the most common cause of hereditary renal amyloidosis in the UK. Patients typically present with kidney impairment and progress to end-stage renal dis...