Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

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Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy

Published:2020-06 Issue:6 Volume:39 Page:317-327
ISSN:2174-2049
Container-title:Revista Portuguesa de Cardiologia (English Edition)
language:en
Short-container-title:Revista Portuguesa de Cardiologia (English Edition)

Author:

Toste Alexandra,Perrot Andreas,Özcelik Cemil,Cardim Nuno

Funder

Charité

Publisher

Elsevier BV

Reference60 articles.

1. Clinical and mechanistic insights into the genetics of cardiomyopathy;Burke;J Am Coll Cardiol,2016

2. Genetics and genomics of single-gene cardiovascular diseases: common hereditary cardiomyopathies as prototypes of single-gene disorders;Marian;J Am Coll Cardiol,2016

3. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC);Elliott;Eur Heart J,2014

4. Formin homology 2 domain containing 3 (FHOD3) is a genetic basis for hypertrophic cardiomyopathy;Ochoa;J Am Coll Cardiol,2018

5. Z-disc genes in hypertrophic cardiomyopathy: stretching the cardiomyopathies?;Bos;J Am Coll Cardiol,2010

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