PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosis-Reference-Cited by-同舟云学术

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PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosis

Published:2015 Issue:2 Volume:8 Page:153
ISSN:0974-2069
Container-title:Annals of Pediatric Cardiology
language:en
Short-container-title:Ann Pediatr Card

Author:

Aggarwal Varun,Dobrolet Nancy,Fishberger Steven,Zablah Jenny,Jayakar Parul,Ammous Zineb

Publisher

Medknow

Subject

Cardiology and Cardiovascular Medicine,Pediatrics, Perinatology and Child Health

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review;International Journal of Molecular Sciences;2024-08-23

2. Echocardiographic Findings in Children of Patients Diagnosed with PRKAG2 Syndrome;Arquivos Brasileiros de Cardiologia;2024-08

3. Achados Ecocardiográficos em Crianças de Pacientes com Diagnóstico de Síndrome do PRKAG2;Arquivos Brasileiros de Cardiologia;2024-08

4. The Genetic Factors Influencing Cardiomyopathies and Heart Failure across the Allele Frequency Spectrum;Journal of Cardiovascular Translational Research;2024-05-21

5. The cardiac conduction system: History, development, and disease;Current Topics in Developmental Biology;2024

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