Transthyretin Val30Met Mutation in an African American With Cardiac Amyloidosis
Author:
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine,Emergency Nursing,Emergency Medicine
Reference16 articles.
1. Evaluation and management of the cardiac amyloidosis;Selvanayagam;J Am Coll Cardiol,2007
2. Variant-sequence transthyretin (isoleucine 122) in late-onset cardiac amyloidosis in black Americans;Jacobson;N Engl J Med,1997
3. Molecular mechanisms of amyloidosis;Merlini;N Engl J Med,2003
4. Mechanisms of amyloidogenesis;Kelly;Nat Struct Biol,2000
5. Kidney and anemia in familial amyloidosis type I;Beirao;Kidney Int,2004
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1. Data-independent acquisition mass spectrometry reveals comprehensive plasma protein profiles in the natural history of patients with hereditary transthyretin amyloidosis (ATTRv);Expert Review of Proteomics;2023-03-04
2. Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis;Neurology and Therapy;2016-02-19
3. A transthyretin variant, Asp18Asn, associated with amyloid cardiomyopathy: a new African-American variant?;Amyloid;2012-11-05
4. An extraordinary ‘sunburn’ in a black patient;British Journal of Dermatology;2011-05-25
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