No-Cost next generation sequencing of nuclear DNA mutations and full mitochondrial DNA sequencing for suspected mitochondrial disease patients.

Mitochondrial diseases are a group of rare, debilitating or fatal genetic disorders that can severely impact daily living and quality of life for patients. Diagnosis can be challenging, with patients often seeing multiple clinicians and experiencing misdiagnosis.

This is a clinician facing program designed to provide suspected mitochondrial disease patients an opportunity for no-cost genetic testing, allowing your patient to get genetic testing for optimal clinical care, which may include potential consideration for ongoing clinical trials.

This program is currently exclusive to providers associated with the Mitochondrial Care Network. As the program expands to the broader clinician community, we’ll notify you via email.