Diseases

Researchers identify rare NAMPT-linked disorder known as MINA syndrome

6. November 2025 Von KI berichtet Bild generiert von KI Fakten geprüft

An international team led by Shinghua Ding at the University of Missouri has identified a rare genetic disorder called Mutation in NAMPT Axonopathy (MINA) syndrome, tied to a mutation in the NAMPT protein that undermines energy production in nerve cells and impairs motor function.