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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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Detalhes bibliográficos
Publicado no:Indian Heart J
Main Authors: Ali, Muzaffar, Bhat, Imtiyaz A., Hafeez, Imran, Dar, Mohd Iqbal, Beig, Jahangir Rashid, Shah, Zafar Amin, Iqbal, Khurshid
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2018
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Acesso em linha: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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