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Clearance of variant transthyretin from serum after liver transplantation in patients with familial amyloidotic polyneuropathy

✍ Scribed by T. Uemichi; J.J. Liepnieks; R.P. Waits; N.L. Ascher; J. Julien; M.D. Benson


Book ID
116168800
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
67 KB
Volume
6
Category
Article
ISSN
0960-8966

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Familial amyloidotic polyneuropathy is an inherited form of amyloidosis associated with a mutant form of a protein called transthyretin. The Methionine-30 variant is the most frequent mutation observed. This disorder is caused by deposition of this protein as amyloid in several organs, such as the h