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Scientists Discover New Genetic Disease Behind Mysterious Muscle Weakness

Mutation in NAMPT Axonopathy (MINA) syndrome causes motor neuron damage by disrupting cellular energy, leading to muscle weakness and coordination loss, researchers report.

Summary by Sci Tech Daily
A University of Missouri-led discovery could pave the way for improved diagnosis and treatment of unexplained movement disorders. An international team of researchers led by Shinghua Ding at the University of Missouri has discovered a new genetic disorder that interferes with muscle control and movement. The condition, known as Mutation in NAMPT Axonopathy (MINA) syndrome, [...]

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BIOENGINEER.ORG broke the news in on Monday, October 27, 2025.
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