Heterozygous junctophilin-2 (JPH2) p.(Thr161Lys) is a monogenic cause for HCM with heart failure-Reference-Cited by-同舟云学术

Heterozygous junctophilin-2 (JPH2) p.(Thr161Lys) is a monogenic cause for HCM with heart failure

Published:2018-09-20 Issue:9 Volume:13 Page:e0203422
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Vanninen Sari U. M.^ORCID,Leivo Krista,Seppälä Eija H.,Aalto-Setälä Katriina,Pitkänen Olli,Suursalmi Piia,Annala Antti-Pekka^ORCID,Anttila Ismo,Alastalo Tero-Pekka,Myllykangas Samuel,Heliö Tiina M.,Koskenvuo Juha W.

Funder

EVO

VTR Fund

Sigrid Juséliuksen Säätiö (FI)

The Academy of Finland

Sigrid Juselius Foundation

Aarne Koskelo Foundation

Sydäntutkimussäätiö

Finnish Foundation for Cardiovascular Research

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference37 articles.

1. Prevalence of hypertrophic cardiomyopathy in a general-population of young-adults—echocardiographic analysis of 4111 subjects in the Cardia Study;BJ Maron;Circulation,1995

2. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases;P Elliott;European Heart Journal,2008

3. Prognosis in hypertrophic cardiomyopathy observed in a large clinic population;MJ Kofflard;American Journal of Cardiology,1993

4. Clinical course of hypertrophic cardiomyopathy in a regional United States cohort;BJ Maron;Jama-Journal of the American Medical Association,1999

5. Catheter ablation for atrial fibrillation in hypertrophic cardiomyopathy: a systematic review and meta-analysis;R Providencia;Heart,2016

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