Phenotypic expression and clinical outcomes in a South Asian PRKAG2 cardiomyopathy cohort

The PRKAG2 syndrome is a rare autosomal dominant phenocopy of sarcomeric hypertrophic cardiomyopathy (HCM), characterized by ventricular pre-excitation, progressive conduction system disease and left ventricular hypertrophy. This study describes the phenotype, genotype and clinical outcomes of a Sou...

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Detalles Bibliográficos
Autores principales: Ahamed, Hisham, Balegadde, Aniketh Vijay, Menon, Shilpa, Menon, Ramesh, Ramachandran, Aishwarya, Mathew, Navin, Natarajan, K. U., Nair, Indu Ramachandran, Kannan, Rajesh, Shankar, Meghna, Mathew, Oommen K., Nguyen, Thong T., Gupta, Ravi, Stawiski, Eric W., Ramprasad, V. L., Seshagiri, Somasekar, Phalke, Sameer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691361/
https://www.ncbi.nlm.nih.gov/pubmed/33244021
http://dx.doi.org/10.1038/s41598-020-77124-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691361/
https://www.ncbi.nlm.nih.gov/pubmed/33244021
http://dx.doi.org/10.1038/s41598-020-77124-9

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