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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...
Shranjeno v:
| izdano v: | Mol Genet Genomic Med |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley and Sons Inc.
2020
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7057083/ https://ncbi.nlm.nih.gov/pubmed/31960626 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1150 |
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