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.
3 Articles
3 Articles
Scientists Discover New Genetic Disease Behind Mysterious Muscle Weakness
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, [...]
Scientists Discover Rare New Genetic Disorder
An international consortium of scientists, spearheaded by Professor Shinghua Ding from the University of Missouri, has uncovered a novel genetic disorder that profoundly impairs motor function and muscle control. This disease, termed Mutation in NAMPT Axonopathy (MINA) syndrome, represents an unprecedented neurological condition caused by mutations in the nicotinamide phosphoribosyltransferase (NAMPT) gene. NAMPT is a […]
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