Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants
Author:
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/13506120500223126
Reference16 articles.
1. Tabulation of human transthyretin (TTR) variants, 2003
2. Variant-Sequence Transthyretin (Isoleucine 122) in Late-Onset Cardiac Amyloidosis in Black Americans
3. Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser
4. Oculoleptomeningeal amyloidosis in a large kindred with a new transthyretin variant Tyr69His
5. LIVER TRANSPLANTATION RESTORES ENDOCRINE CELLS IN PATIENTS WITH FAMILIAL AMYLOIDOTIC POLYNEUROPATHY1
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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. Effect of alanine versus serine at position 88 of human transthyretin mutants on the protein stability;Protein Engineering, Design and Selection;2023
3. Familial Amyloidotic Polyneuropathy with Leptomeningeal and Cardiac Involvement in a Patient with Gly73Glu Transthyretin Gene Mutation — Non-invasive Diagnostic Approach with Multimodality Imaging Findings: a Case Report;Hong Kong Journal of Radiology;2022-09-26
4. Clinical Profile and Prognosis of Hereditary Transthyretin Amyloid Cardiomyopathy: A Single-Center Study in South China;Frontiers in Cardiovascular Medicine;2022-06-27
5. Treatment of transthyretin His88Arg amyloidosis with RNA interference therapy: A case report;Journal of Cardiology Cases;2022-06
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