Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot.

Kheirollahi, Majid; Khosravi, Fereshteh; Ashouri, Saeideh; Ahmadi, Alireza

Kheirollahi, Majid; Khosravi, Fereshteh; Ashouri, Saeideh; Ahmadi, Alireza.

Afiliación

Kheirollahi M; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan, Iran; Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Khosravi F; Department of Biology, Islamic Azad University, Yazd, Iran.
Ashouri S; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan, Iran.
Ahmadi A; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan, Iran.

J Res Med Sci ; 21: 24, 2016.

Article en En | MEDLINE | ID: mdl-27904570

Palabras clave

Cardiac defect; Iranian patient; NKX2.5 gene; tetralogy of Fallot (TOF)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Res Med Sci Año: 2016 Tipo del documento: Article País de afiliación: Irán Pais de publicación: India

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