Cutis laxa in hereditary gelsolin amyloidosis
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2004.06276.x/fullpdf
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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
3. Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies
4. Gelsolin-related spinal and cerebral amyloid angiopathy
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