Hereditary amyloidosis caused by R554L fibrinogen Aα-chain mutation in a Spanish family and review of the literature-Reference-Cited by-同舟云学术

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Hereditary amyloidosis caused by R554L fibrinogen Aα-chain mutation in a Spanish family and review of the literature

Published:2013-04-03 Issue:2 Volume:20 Page:72-79
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Haidinger Michael,Werzowa Johannes,Kain Renate,Antlanger Marlies,Hecking Manfred,Pfaffenberger Stefan,Mascherbauer Julia,Gremmel Thomas,Gilbertson Janet A.,Rowczenio Dorota,Weichhart Thomas,Kopecky Chantal,Hörl Walter H.,Hawkins Philip N.,Säemann Marcus D.

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/13506129.2013.781998

Reference20 articles.

1. Molecular Mechanisms of Amyloidosis

2. New insights into systemic amyloidosis: the importance of diagnosis of specific type

3. Hereditary renal amyloidosis associated with a mutant fibrinogen α–chain

4. Nephrotic Syndrome Due to an Amyloidogenic Mutation in Fibrinogen A α Chain

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