Mitochondrial Diseases Panel
Mitochondrial Diseases Panel
Regular price
€29.00 EUR
Regular price
Sale price
€29.00 EUR
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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.
List of main conditions:
See more about the product
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
This product is only meant for customers who already purchased a MyGenome Test