Mutant fibrinogen A-α-chain associated with hereditary renal amyloidosis and peripheral neuropathy-Reference-Cited by-同舟云学术

Mutant fibrinogen A-α-chain associated with hereditary renal amyloidosis and peripheral neuropathy

Published:2004-09 Issue:3 Volume:11 Page:200-207
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

de Carvalho Mamede,Linke Reinhold P,Domingos Fernando,Evangelista Teresinha,Ducla-Soares José Luís,Nathrath Walter BJ,Azevedo-Coutinho Conceição,Lima Raquel,Saraiva Maria João

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/13506120400000772

Reference17 articles.

1. Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.

2. A New Human Hereditary Amyloidosis: The Result of a Stop-Codon Mutation in the Apolipoprotein AII Gene

3. Human lysozyme gene mutations cause hereditary systemic amyloidosis

4. Hereditary renal amyloidosis with a novel variant fibrinogen.

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