Mutational Assessment in NKX2-5 and ACTC1 Genes in Patients with Congenital Cardiac Septal Defect (CCSD) from Ethnic Kashmiri Population

(1) Background globe. The etiology of CHDs is complex and involves both genetic and non-genetic factors. Although, significant progress has been made in deciphering the genetic components involved in CHDs, recent reports have revealed that mutations in Nk2 homeobox5 (NKX2-5) and actin alpha cardiac...

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Detalles Bibliográficos
Autores principales: Nazeer, Nadeem Ul, Bhat, Mohammad Akbar, Rah, Bilal, Bhat, Gh Rasool, Wani, Shadil Ibrahim, Yousuf, Adfar, Dar, Abdul Majeed, Afroze, Dil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408331/
https://www.ncbi.nlm.nih.gov/pubmed/36011517
http://dx.doi.org/10.3390/ijerph19169884

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408331/
https://www.ncbi.nlm.nih.gov/pubmed/36011517
http://dx.doi.org/10.3390/ijerph19169884

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