Skip to product information
1 of 1

Mitochondrial Diseases Panel

Mitochondrial Diseases Panel

Regular price €49.00 EUR
Regular price Sale price €49.00 EUR
Sale Sold out
This product is only meant for customers who already purchased a MyGenome Test

The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major mitochondrial conditions

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • More than 125 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Kearns-Sayre syndrome
  • Leber hereditary optic neuropathy
  • Leigh syndrome
  • Mitochondrial complex III deficiency
  • Mitochondrial encephalomyopathy
See more about the product

This product is only meant for customers who already purchased a MyGenome Test