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.

Heidari, Mohammad Mehdi; Khatami, Mehri; Kamalipour, Akram; Kalantari, Mustafa; Movahed, Mahsa; Emmamy, Mohammad Hayet; Hadadzadeh, Mehdi; Bragança, José; Namnabat, Mohsen; Mazrouei, Bahareh

Heidari, Mohammad Mehdi; Khatami, Mehri; Kamalipour, Akram; Kalantari, Mustafa; Movahed, Mahsa; Emmamy, Mohammad Hayet; Hadadzadeh, Mehdi; Bragança, José; Namnabat, Mohsen; Mazrouei, Bahareh.

Afiliación

Heidari MM; Department of Biology, Yazd University, Yazd, Iran.
Khatami M; Department of Biology, Yazd University, Yazd, Iran.
Kamalipour A; Department of Biology, Yazd University, Yazd, Iran.
Kalantari M; Department of Biology, Yazd University, Yazd, Iran.
Movahed M; Department of Biology, Yazd University, Yazd, Iran.
Emmamy MH; Department of Biology, Yazd University, Yazd, Iran.
Hadadzadeh M; Department of Cardiac Surgery, Afshar Hospital, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Bragança J; Faculty of Medicine and Biomedical Sciences, Algarve Biomedical Center Research Institute, University of Algarve, Faro, Portugal.
Namnabat M; Department of Biology, Yazd University, Yazd, Iran.
Mazrouei B; Department of Biology, Yazd University, Yazd, Iran.

EXCLI J ; 21: 1306-1330, 2022.

Article en En | MEDLINE | ID: mdl-36483916

Palabras clave

congenital heart disease; in-silico analysis; mitochondrial genome; mt-tRNA; mutation

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: EXCLI J Año: 2022 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Alemania

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