A new heterozygous G duplicate in exon1 (c.100dupG) of gelsolin gene causes Finnish gelsolin amyloidosis in a Chinese family
Author:
Affiliation:
1. Department of Neurology; The First Hospital, Jilin University; Jinlin China
2. Department of Internal Medicine; The center Hospital of Gongzhuling; Jilin China
Publisher
Wiley
Subject
Behavioral Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/brb3.1151/fullpdf
Reference14 articles.
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2. Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187;Chapelle;Nature Genetics,1992
3. Hereditary gelsolin amyloidosis mimicking Sjögren’s syndrome;Juusela;Clinical Rheumatology,2009
4. Familial amyloidosis of the Finnish type (FAF);Kiuru;Acta Neurologica Scandinavica,1992
5. Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide;Kiuru;Amyloid,1998
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