LEIGH SYNDROME MITOCHONDRIAL MUTATION DETECTION

This test is useful for elucidation of mitochondrial mutations linked to the mitochondrial disease Leigh Syndrome.

  • 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