Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: A case report
Author:
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/13506120601116393
Reference35 articles.
1. Gelsolin-related familial amyloidosis, Finnish type (FAF), and its variants found worldwide
2. Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family
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