Familial right ventricular dilated cardiomyopathy.
Cardiomyopathy of unknown cause occurred in three of six siblings. The course of the illness was marked by life threatening supraventricular and ventricular arrhythmias, sinoatrial block, atrioventricular block, and embolism (in one patient). The disease was characterised by right ventricular dilata...
保存先:
| 出版年: | Br Heart J |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
1985
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC481871/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4015925/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/hrt.54.2.156 |
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