CONNEXIN 26 MUTATION DETECTION
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 2% of all genetic hearing loss and 1% of all childhood hearing loss.

Sample Type - Blood

Reporting Time - Please Call Customer care

Prerequisites - No special preparation required

Price - ₹8230/-

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