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Congenital septal defects in Karachi, Pakistan: an update of mutational screening by high-resolution melting (HRM) analysis of MTHFR C677T.

Syed Irtiza AliObaid Yusuf KhanNadir NaveedHussain AhmadNajma PatelAfsheen Arif
Published in: Human genomics (2024)
rs1801133 has lack of significant association with congenital septal defects. The absence of TT genotype in this study suggesting the role of natural selection in targeted population. HRM is an easy, fast and next generation of PCR, which may be used for applied genomics.
Keyphrases
  • high resolution
  • tertiary care
  • hypertrophic cardiomyopathy
  • single cell
  • heart failure
  • left ventricular
  • tandem mass spectrometry
  • high speed
  • atrial fibrillation