<italic>In Silico</italic> Investigation of CACNA2D1 S755T Mutation Associated With Short QT Syndrome
Short QT syndrome (SQTS) is a genetic disease characterized by constantly short QT intervals and high risks of sudden death. SQTS6 is one of the identified SQTS genotype variants associated with the <italic>CACNA2D1</italic> S755T mutation. However, the pathogenesis of SQTS induced arrhy...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
IEEE
2021-01-01
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| Series: | IEEE Access |
| Subjects: | |
| Online Access: | https://ieeexplore.ieee.org/document/9437192/ |