GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
Background: Brugada syndrome (BrS) is a rare inherited disease causing sudden cardiac death (SCD). Copy number variants (CNVs) can contribute to disease susceptibility, but their role in Brugada syndrome (BrS) is unknown. We aimed to identify a CNV associated with BrS and elucidated its clinical imp...
Збережено в:
| Автори: | , , , , , , , , , , , , , , , , , |
|---|---|
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Elsevier
2020-07-01
|
| Серія: | EBioMedicine |
| Предмети: | |
| Онлайн доступ: | http://www.sciencedirect.com/science/article/pii/S2352396420302188 |
| Теги: |
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|