CONNEXIN 26 MUTATION DETECTION

Connexin 26 (Cx26) is a protein found on the (GJB2) gene and is the most common cause of congenital sensorineural hearing loss. Connexin 26 mutations are responsible for at least 20% of all genetic hearing loss and 10% of all childhood hearing loss.

  • Test Type:
  • Pre-test Information:
    No Special preparation required
  • Report Delivery:
    Sample by Sat 11 am; Report 13 days
  • Components:
    0