Abstract
Background Congenital tooth agenesis (CTA), a type of craniofacial disorders affects approximately 20% (including 3 molar or Wisdom teeth) and 2-10% (excluding 3 molar) of the world population. Five major candidate genes known to be associated with syndromic and non-syndromic CTA, these are PAX9, MSX1, AXIN2, EDA and WNT10A. The present investigation was undertaken to identify and characterize disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis
Highlights
Congenital tooth agenesis (CTA), a type of craniofacial disorders affects approximately 20% and 2-10% of the world population
Identification and characterization of disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis
The present investigation was undertaken to identify and characterize disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis
Summary
Congenital tooth agenesis (CTA), a type of craniofacial disorders affects approximately 20% (including 3rd molar or Wisdom teeth) and 2-10% (excluding 3rd molar) of the world population. Identification and characterization of disease causing genetic variant by conventional genotyping and whole genome sequencing in familial tooth agenesis Background Congenital tooth agenesis (CTA), a type of craniofacial disorders affects approximately 20% (including 3rd molar or Wisdom teeth) and 2-10% (excluding 3rd molar) of the world population.
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