Research Study on Mitochondrial Diseases: Investigation of Mitochondrial Diseases Due to Nuclear Gene Mutations

Overview

About this study

This research is being done to better understand how mitochondrial diseases show themselves and to find the abnormal gene(s) causing these diseases.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Male and female subjects with age between 0 and 99 years
  • Have a mitochondrial disease or suspected mitochondrial disease, or you are the relative of a person with a mitochondrial disease
  • Lack of mitochondrial DNA mutations

Exclusion Criteria:

  • Known disease-causing mutation and lack of neurological manifestations.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Margherita Milone, M.D., Ph.D.

Closed for enrollment

Contact information:

Delana Weis CCRP

(507)266-7196

weis.delana@mayo.edu

More information

Publications

Publications are currently not available