Diseases

Researchers identify rare NAMPT-linked disorder known as MINA syndrome

6 ноября 2025 Сообщено ИИ Изображение, созданное ИИ Проверено фактами

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.