Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations

BACKGROUND: Autosomal dominantly inherited PRKAG2 cardiac syndrome is due to a unique defect of the cardiac cell metabolism and has a distinctive histopathology with excess intracellular glycogen, and prognosis different from sarcomeric hypertrophic cardiomyopathy. We aimed to define the distinct ch...

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Detalles Bibliográficos
Autores principales: Pöyhönen, Pauli, Hiippala, Anita, Ollila, Laura, Kaasalainen, Touko, Hänninen, Helena, Heliö, Tiina, Tallila, Jonna, Vasilescu, Catalina, Kivistö, Sari, Ojala, Tiina, Holmström, Miia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619453/
https://www.ncbi.nlm.nih.gov/pubmed/26496977
http://dx.doi.org/10.1186/s12968-015-0192-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619453/
https://www.ncbi.nlm.nih.gov/pubmed/26496977
http://dx.doi.org/10.1186/s12968-015-0192-3

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