MITOCHONDRIAL MUTATION DETECTION COMPREHENSIVE PANEL

This test is useful for elucidation of mitochondrial mutations linked to various mitochondrial diseases such as mitochondrial myopathy, MELAS, MERFF, LHON, LEIGH syndrome, Deafness etc.

  • Test Type:
  • Pre-test Information:
    Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
  • Report Delivery:
    Sample Mon by 9 am; Report Fri
  • Components:
    0