Novel gelsolin variant as the cause of nephrotic syndrome and renal amyloidosis in a large kindred-Reference-Cited by-同舟云学术

Novel gelsolin variant as the cause of nephrotic syndrome and renal amyloidosis in a large kindred

Published:2014-03-06 Issue:2 Volume:21 Page:110-112
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Efebera Yvonne A.,Sturm Amy,Baack Elizabeth C.,Hofmeister Craig C.,Satoskar Anjali,Nadasdy Tibor,Nadasdy Gyongyi,Benson Don M.,Gillmore Julian D.,Hawkins Philip N.,Rowczenio Dorota

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/13506129.2014.891502

Reference7 articles.

1. Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention

2. Familial amyloid polyneuropathy (Finnish type) in a Japanese family: Clinical features and immunocytochemical studies

3. Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type

4. Laser microdissection and mass spectrometry–based proteomics aids the diagnosis and typing of renal amyloidosis

5. Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East

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