Loading...

Diagnosis, Pathogenesis, Treatment, and Prognosis of Hereditary Fibrinogen Aα-Chain Amyloidosis

Mutations in the fibrinogen Aα-chain gene are the most common cause of hereditary renal amyloidosis in the United Kingdom. Previous reports of fibrinogen Aα-chain amyloidosis have been in isolated kindreds, usually in the context of a novel amyloidogenic mutation. Here, we describe 71 patients with...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Gillmore, Julian D., Lachmann, Helen J., Rowczenio, Dorota, Gilbertson, Janet A., Zeng, Cai-Hong, Liu, Zhi-Hong, Li, Lei-Shi, Wechalekar, Ashutosh, Hawkins, Philip N.
Format: Artigo
Sprog:Inglês
Udgivet: American Society of Nephrology 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2637055/
https://ncbi.nlm.nih.gov/pubmed/19073821
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2008060614
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!