Diseases

关注
Illustration of scientists in a lab discovering MINA syndrome, a rare genetic disorder affecting nerve cells and motor function.
AI 生成的图像

Researchers identify rare NAMPT-linked disorder known as MINA syndrome

由 AI 报道 AI 生成的图像 事实核查

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.

此网站使用 cookie

我们使用 cookie 进行分析以改进我们的网站。阅读我们的 隐私政策 以获取更多信息。
拒绝