PRADER-WILLI SYNDROME MUTATION DETECTION, METHYLATION SPECIFIC PCR
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are clinically distinct neurodevelopmental genetic disorders that map to 15q11-q13. The primary phenotypes are attributable to loss of expression of imprinted genes within this region which can arise by means of a number of mechanisms. The most sensitive single approach to diagnosing both PWS and AS is to study methylation patterns within 15q11-q13.
Parameter(s) covered : 1
Report Frequency: Sample Sat by 11 am; Report 12 Working days
Special Instruction: Physician prescription is mandatory.
Price : ₹ 9600.00
Parameters
- PRADER WILLI SYNDROME DETECTION BY METHYLATION