Functional characterization of a novel JPH2 variant (p.R160H) associated with dilated cardiomyopathy
Abstract Background Dilated cardiomyopathy (DCM) is a genetic cardiac disorder characterized by ventricular dilation and systolic dysfunction. Mutations in calcium-handling genes such as JPH2, which plays a critical role in maintaining cardiac dyad integrity, have been associated with DCM. Although...
I tiakina i:
| Ngā kaituhi matua: | , , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
BMC
2025-12-01
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| Rangatū: | BMC Cardiovascular Disorders |
| Ngā marau: | |
| Urunga tuihono: | https://doi.org/10.1186/s12872-025-05443-8 |
| Ngā Tūtohu: |
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