Spectrum of hereditary transthyretin amyloidosis due to T60A(p.Thr80Ala) variant in an Irish Amyloidosis Network

Background Variant transthyretin amyloidosis (ATTRv) is a hereditary multisystem disorder with clinical spectrum ranging from predominant cardiomyopathy to polyneuropathy. In the Irish population, the T60A mutation has been previously recognised as the most common genotype.Objectives The aim of this...

Full description

Saved in:
Bibliographic Details
Main Authors: Michael Alexander, Sinéad M Murphy, Katie Murphy, Emer Joyce, Neasa Starr, Katie Hewitt, Zara Togher, Saadah Sulong, Joseph P Morris, Mark Coyne, Gerard Giblin
Format: Article
Language:English
Published: BMJ Publishing Group 2024-11-01
Series:Open Heart
Online Access:https://openheart.bmj.com/content/11/2/e002906.full
Tags: Add Tag
No Tags, Be the first to tag this record!