Diseases

Fuatilia
Illustration of scientists in a lab discovering MINA syndrome, a rare genetic disorder affecting nerve cells and motor function.
Àwòrán tí AI ṣe

Researchers identify rare NAMPT-linked disorder known as MINA syndrome

Ti AI ṣe iroyin Àwòrán tí AI ṣe Ti ṣayẹwo fun ododo

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.

Ojú-ìwé yìí nlo kuki

A nlo kuki fun itupalẹ lati mu ilọsiwaju wa. Ka ìlànà àṣírí wa fun alaye siwaju sii.
Kọ