SPINAL MUSCULAR ATROPHY (SMA), CARRIER DETECTION
SMA of all types is associated with homozygous mutations in the survival motor neuron 1 gene (SMN1). This test detects homozygous deletion of SMN1 Exon 7 and or Exon 8 which accounts for 95% of SMA. It detects both active and carrier status of the disease.
Parameter(s) covered : 4
Report Frequency: Sample Mon by 11 am; Report Sat
Special Instruction: Physician prescription is mandatory.
Price : ₹ 4300.00
Parameters
- SMN1 Exon 7
- SMN1 Exon 8
- SMN2 Exon 7
- SMN2 Exon 8