Assessing the Role of Mitochondrial Dysfunction in Primary Progressive Multiple Sclerosis
IRCCS San Raffaele
140 participants
Sep 20, 2021
OBSERVATIONAL
Conditions
Summary
The purpose of this project is to study genetic determinants of mitochondrial impairment in primary progressive multiple sclerosis. Specific aims are: 1) identify mitochondrial-related pathways, inherited and somatic mitochondrial DNA mutations associated to primary progressive multiple sclerosis, 2) functionally assess the identified genetic alterations.
Eligibility
Plain Language Summary
Simplified for easier understanding
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Locations(2)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06025903