Xerostomia in hereditary gelsolin amyloidosis
Author:
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/13506129.2013.764284
Reference42 articles.
1. Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy
2. Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: A case report
3. Gelsolin Amyloidosis as a Cause of Early Aging and Progressive Bilateral Facial Paralysis
4. Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease
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