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Role of Non-Coding Variants in Brugada Syndrome
Brugada syndrome (BrS) is an inherited electrical heart disease associated with a high risk of sudden cardiac death (SCD). The genetic characterization of BrS has always been challenging. Although several cardiac ion channel genes have been associated with BrS, SCN5A is the only gene that presents d...
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| Udgivet i: | Int J Mol Sci |
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| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7698069/ https://ncbi.nlm.nih.gov/pubmed/33202810 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21228556 |
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