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Prevalence of TTR variants detected by whole-exome sequencing in hypertrophic cardiomyopathy (2019)

First Author: Lopes L

Attributed to: Discovering the causes of mutation-negative hypertrophic cardiomyopathy funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1080/13506129.2019.1665996

PubMed Identifier: 31554435

Publication URI: http://europepmc.org/abstract/MED/31554435

Type: Journal Article/Review

Parent Publication: Amyloid

Issue: 4

ISSN: 1350-6129