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.
Parameter(s) covered : 1
Report Frequency: Sample Sat by 11 am; Report 13 Working days
Special Instruction: Duly filled Nx Gen Sequencing (NGS) Test Requisition Form (Form 40) is mandatory.
Price : ₹ 9800.00
Parameters
- CONNEXIN 26 MUTATION DETECTION BY PCR