PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders-Reference-Cited by-同舟云学术

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PRKAG2 syndrome, a rare hypertrophic cardiomyopathy: a Brazilian long-term follow-up with extracardiac disorders

Published:2024 Issue: Volume:22 Page:
ISSN:1679-4508
Container-title:einstein (São Paulo)
language:en
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Author:

van der Steld Lenises de Paula^ORCID,Rocha Mario de Seixas^ORCID,Ladeia Ana Marice Teixeira^ORCID,Livramento Humberto Lago^ORCID,Campos Gervásio Batista^ORCID,Darrieux Francisco Carlos da Costa^ORCID,Campuzano Oscar^ORCID,Brugada Ramon^ORCID

Publisher

Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein

Reference20 articles.

1. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome;Gollob;N Engl J Med,2001

2. Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family;van der Steld;Am J Case Rep,2017

3. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy;Gollob;Curr Opin Cardiol,2002

4. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy;Arad;J Clin Invest,2002

5. Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis;Lopez-Sainz;J Am Coll Cardiol,2020

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