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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Dettagli Bibliografici
Pubblicato in:Indian Heart J
Autori principali: Ali, Muzaffar, Bhat, Imtiyaz A., Hafeez, Imran, Dar, Mohd Iqbal, Beig, Jahangir Rashid, Shah, Zafar Amin, Iqbal, Khurshid
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elsevier 2018
Soggetti:
Cardiac Electrophysiology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6034022/
https://ncbi.nlm.nih.gov/pubmed/29961461
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ihj.2017.10.010
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