Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole‐exome sequencing
Abstract Background The aim of this study was to identify the genetic causes of patients with hypertrophic cardiomyopathy (HCM) within a family. Most of the previous studies found point mutations as the genetic causes for HCM, whole‐gene deletion was rarely reported. Methods Although, clinical genet...
| Автори: | , , , , |
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| Формат: | Стаття |
| Мова: | English |
| Опубліковано: |
Wiley
2020-03-01
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| Серія: | Molecular Genetics & Genomic Medicine |
| Предмети: | |
| Онлайн доступ: | https://doi.org/10.1002/mgg3.1150 |