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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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| Publicado no: | Indian Heart J |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2018
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| Assuntos: | |
| 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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