Cargando…
An Update on MYBPC3 Gene Mutation in Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is the most prevalent genetically inherited cardiomyopathy that follows an autosomal dominant inheritance pattern. The majority of HCM cases can be attributed to mutation of the MYBPC3 gene, which encodes cMyBP-C, a crucial structural protein of the cardiac muscle....
Autores principales: | Tudurachi, Bogdan-Sorin, Zăvoi, Alexandra, Leonte, Andreea, Țăpoi, Laura, Ureche, Carina, Bîrgoan, Silviu Gabriel, Chiuariu, Traian, Anghel, Larisa, Radu, Rodica, Sascău, Radu Andy, Stătescu, Cristian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341819/ https://www.ncbi.nlm.nih.gov/pubmed/37445689 http://dx.doi.org/10.3390/ijms241310510 |
Ejemplares similares
-
From Classic to Modern Prognostic Biomarkers in Patients with Acute Myocardial Infarction
por: Stătescu, Cristian, et al.
Publicado: (2022) -
Assessment of Inflammatory Hematological Ratios (NLR, PLR, MLR, LMR and Monocyte/HDL–Cholesterol Ratio) in Acute Myocardial Infarction and Particularities in Young Patients
por: Tudurachi, Bogdan-Sorin, et al.
Publicado: (2023) -
A Systematic Review on the Risk Modulators of Myocardial Infarction in the “Young”—Implications of Lipoprotein (a)
por: Stătescu, Cristian, et al.
Publicado: (2023) -
The Challenge of High Coronary Thrombotic Events in Patients with ST-Segment Elevation Myocardial Infarction and COVID-19
por: Anghel, Larisa, et al.
Publicado: (2022) -
Cardiac Resynchronization Therapy in Non-Ischemic Cardiomyopathy: Role of Multimodality Imaging
por: Stătescu, Cristian, et al.
Publicado: (2021)