Natural History Study of FDXR Mutation-related Mitochondriopathy

CompletedOBSERVATIONAL
Enrollment

33

Participants

Timeline

Start Date

November 3, 2020

Primary Completion Date

August 17, 2023

Study Completion Date

August 17, 2023

Conditions
Neurodegenerative Disease, HereditaryMitochondrial DiseasesOptic Atrophy
Interventions
GENETIC

Mutation analysis

The investigators will sequence DNA samples from the patients or their families.

Trial Locations (1)

14203

UBMD Pediatrics, Buffalo

All Listed Sponsors
collaborator

The Callum McKeefery and Nikki Albano McKeefery Pediatric Division of Genetics Fund

UNKNOWN

lead

State University of New York at Buffalo

OTHER

NCT04580979 - Natural History Study of FDXR Mutation-related Mitochondriopathy | Biotech Hunter | Biotech Hunter