CONNEXIN 30 MUTATION DETECTION
Useful to identify a second mutation in patients who carry a single CX26 mutation and to determine the genetic basis for hearing loss in an affected individual.
Parameter(s) covered : 1
Report Frequency: Sample Sat by 11 am; Report 15 Working days
Special Instruction: Duly filled Nx Gen Sequencing (NGS) Test Requisition Form (Form 40) is mandatory.
Price : ₹ 6800.00
Parameters
- CONNEXIN 30 MUTATION DETECTION BY PCR-SEQUENCING