Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs)
Abstract 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...
Main Authors: | Sumbal Sarwar, Shabana, Khadija Sajjad, Shahida Hasnain |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2023-02-01
|
Series: | BMC Pediatrics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12887-023-03851-3 |
Similar Items
-
Congenital tunnel‐shaped ventricular septal defect
by: Mohammad Reza Eftekhari, et al.
Published: (2023-12-01) -
Case report of combined correction of postinfarction ventricular septal defect
by: О. П. Лукин, et al.
Published: (2015-10-01) -
Percutaneous transcatheter closure of atrial and ventricular septal defect in the same session
by: Atila İyisoy, et al.
Published: (2014-04-01) -
Circulating microRNA: Myocardium-derived prenatal biomarker of ventricular septal defects
by: Yiru Yang, et al.
Published: (2022-08-01) -
Transcatheter Closure of Cardiac Defects with Lifetech™ Konar-MultifunctionalOccluder Experience in a Tertiary Care Center
by: Andaleeb Ara, et al.
Published: (2022-11-01)