Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality

BACKGROUND: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is associated with ventricular arrhythmia, heart failure (HF), and sudden death. Thromboembolism is also an important and serious complication of ARVC/D. However, the etiology of ARVC/D and thromboembolism and their assoc...

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Detalles Bibliográficos
Autores principales: Chen, Jia, Ma, Yuting, Li, Hong, Lin, Zhuo, Yang, Zhe, Zhang, Qin, Wang, Feng, Lin, Yanping, Ye, Zebing, Lin, Yubi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077868/
https://www.ncbi.nlm.nih.gov/pubmed/35526016
http://dx.doi.org/10.1186/s13023-022-02348-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9077868/
https://www.ncbi.nlm.nih.gov/pubmed/35526016
http://dx.doi.org/10.1186/s13023-022-02348-z

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