Clinical profile in arrhythmogenic cardiomyopathy and a recessive plakophilin-2 gene mutation

OBJECTIVE: Arrhythmogenic cardiomyopathy (ACM) is not an uncommon cause of cardiac morbidity in Kashmir valley. This study was designed to document various clinical features and to sequence exons 11 and 12 of plakophilin 2 (PKP2) gene in these patients. METHODS: ACM patients who attended cardiology...

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Detalles Bibliográficos
Autores principales: Ali, Muzaffar, Bhat, Imtiyaz A., Hafeez, Imran, Dar, Mohd Iqbal, Beig, Jahangir Rashid, Shah, Zafar Amin, Iqbal, Khurshid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Cardiac Electrophysiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034022/
https://www.ncbi.nlm.nih.gov/pubmed/29961461
http://dx.doi.org/10.1016/j.ihj.2017.10.010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034022/
https://www.ncbi.nlm.nih.gov/pubmed/29961461
http://dx.doi.org/10.1016/j.ihj.2017.10.010

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