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Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole‐exome sequencing
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 genetic test...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057083/ https://www.ncbi.nlm.nih.gov/pubmed/31960626 http://dx.doi.org/10.1002/mgg3.1150 |