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Clinical disease presentation and ECG characteristics of LMNA mutation carriers
OBJECTIVE: Mutations in the LMNA gene encoding lamins A and C of the nuclear lamina are a frequent cause of cardiomyopathy accounting for 5–8% of familial dilated cardiomyopathy (DCM). Our aim was to study disease onset, presentation and progression among LMNA mutation carriers. METHODS: Clinical fo...
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| Опубликовано в: : | Open Heart |
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| Главные авторы: | , , , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BMJ Publishing Group
2017
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5255551/ https://ncbi.nlm.nih.gov/pubmed/28123761 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/openhrt-2016-000474 |
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