Use App for best experience!
Available for Android & iOS
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.
Duly filled Genomics Clinical information requisition form is mandatory.
Available on: