A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells
Author:
Affiliation:
1. Department of Pathology, National Cardiovascular Center, Osaka,
2. Third Department of Internal Medicine, Miyazaki Medical College, Miyazaki and
3. Department of Cardiology, National Cardiovascular Center, Osaka, Japan
Publisher
Wiley
Subject
General Medicine,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1440-1827.1999.00962.x
Reference16 articles.
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3. Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE‐122).;Nichols WC;J. Lab. Clin. Med.,1991
4. A new transthyretin mutation associated with amyloid cardiomyopathy.;Saraiva MJM;Am. J. Hum. Genet.,1992
5. A New Prealbumin Variant in Familial Amyloid Cardiomyopathy of Danish Origin
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