Mitochondrial Cardiomyopathy: Molecular Epidemiology, Diagnosis, Models, and Therapeutic Management

Mitochondrial cardiomyopathy (MCM) is characterized by abnormal heart-muscle structure and function, caused by mutations in the nuclear genome or mitochondrial DNA. The heterogeneity of gene mutations and various clinical presentations in patients with cardiomyopathy make its diagnosis, molecular me...

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Detalles Bibliográficos
Autores principales: Yang, Jinjuan, Chen, Shaoxiang, Duan, Fuyu, Wang, Xiuxiu, Zhang, Xiaoxian, Lian, Boonxuan, Kou, Meng, Chiang, Zhixin, Li, Ziyue, Lian, Qizhou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655095/
https://www.ncbi.nlm.nih.gov/pubmed/36359908
http://dx.doi.org/10.3390/cells11213511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655095/
https://www.ncbi.nlm.nih.gov/pubmed/36359908
http://dx.doi.org/10.3390/cells11213511

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