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Published in 2023 at "Expert Review of Proteomics"
DOI: 10.1080/14789450.2023.2195096
Abstract: ABSTRACT Objectives Hereditary transthyretin amyloidosis (ATTRv) is a rare, fatal, autosomal dominant disease with more than 140 mutations discovered. Three phenotypes of amyloid infiltration are neuropathy (ATTRv-PN), cardiopathy (ATTRv-CM), and neuropathy + cardiopathy (ATTRv-MIX). The…
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Keywords:
attrv;
data independent;
amyloidosis attrv;
hereditary transthyretin ... See more keywords
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Published in 2022 at "Current neuropharmacology"
DOI: 10.2174/1570159x21666221108094736
Abstract: Variant Transthyretin Amyloidosis (ATTRv) neuropathy is an adult-onset, autosomal dominant, lethal, multisystemic disease due to the deposition of mutated transthyretin (TTR) in various organs, commonly involving the peripheral nerves and the heart. Circulating TTR tetramers…
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Keywords:
variant transthyretin;
amyloidosis attrv;
gene;
transthyretin amyloidosis ... See more keywords