Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease

Background and objective: Congenital heart disease (CHD) is the most common birth abnormality in the structure or function of the heart that affects approximately 1% of all newborns. Despite its prevalence and clinical importance, the etiology of CHD remains mainly unknown. Somatic and germline muta...

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Detalles Bibliográficos
Autores principales: Khatami, Mehri, Mazidi, Mansoureh, Taher, Shabnam, Heidari, Mohammad Mehdi, Hadadzadeh, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122093/
https://www.ncbi.nlm.nih.gov/pubmed/30344277
http://dx.doi.org/10.3390/medicina54030046

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122093/
https://www.ncbi.nlm.nih.gov/pubmed/30344277
http://dx.doi.org/10.3390/medicina54030046

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