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A novel αB-crystallin R123W variant drives hypertrophic cardiomyopathy by promoting maladaptive calcium-dependent signal transduction
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disorder affecting 1 in 500 people in the general population. Characterized by asymmetric left ventricular hypertrophy, cardiomyocyte disarray and cardiac fibrosis, HCM is a highly complex disease with heterogenous clinica...
Autores principales: | Chou, Chun, Martin, Gregory L., Perera, Gayani, Awata, Junya, Larson, Amy, Blanton, Robert, Chin, Michael T. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10331725/ https://www.ncbi.nlm.nih.gov/pubmed/37435054 http://dx.doi.org/10.3389/fcvm.2023.1223244 |
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