Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs)

BACKGROUND: With prevalence up to 4%, Ventricular Septal Defect (VSD) is one of the leading causes of neonatal deaths. VSD is a common complex genetic disorder that has been associated with many genetic determinants. Variants from genes for the transcription factors including T-Box TBX5 and NFATc1 (...

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Detalles Bibliográficos
Autores principales: Sarwar, Sumbal, Shabana, Sajjad, Khadija, Hasnain, Shahida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909889/
https://www.ncbi.nlm.nih.gov/pubmed/36759823
http://dx.doi.org/10.1186/s12887-023-03851-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9909889/
https://www.ncbi.nlm.nih.gov/pubmed/36759823
http://dx.doi.org/10.1186/s12887-023-03851-3

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