Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease

Most studies aiming at unraveling the molecular events associated with cardiac congenital heart disease (CHD) have focused on the effect of mutations occurring in the nuclear genome. In recent years, a significant role has been attributed to mitochondria for correct heart development and maturation...

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Detalles Bibliográficos
Autores principales: Heidari, Mohammad Mehdi, Khatami, Mehri, Kamalipour, Akram, Kalantari, Mustafa, Movahed, Mahsa, Emmamy, Mohammad Hayet, Hadadzadeh, Mehdi, Bragança, José, Namnabat, Mohsen, Mazrouei, Bahareh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727243/
https://www.ncbi.nlm.nih.gov/pubmed/36483916
http://dx.doi.org/10.17179/excli2022-5298

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727243/
https://www.ncbi.nlm.nih.gov/pubmed/36483916
http://dx.doi.org/10.17179/excli2022-5298

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