Diseases

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

Researchers identify rare NAMPT-linked disorder known as MINA syndrome

November 06, 2025 በAI የተዘገበ በ AI የተሰራ ምስል እውነት ተፈትሸ

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.

ይህ ድረ-ገጽ ኩኪዎችን ይጠቀማል

የእኛን ጣቢያ ለማሻሻል ለትንታኔ ኩኪዎችን እንጠቀማለን። የእኛን የሚስጥር ፖሊሲ አንብቡ የሚስጥር ፖሊሲ ለተጨማሪ መረጃ።

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