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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 (...
Autores principales: | Sarwar, Sumbal, Shabana, Sajjad, Khadija, Hasnain, Shahida |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
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 |
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