Diagnosis of Charcot-Marie-Tooth Disease

Armen Hareyan's picture
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Hereditary Charcot-Marie-Tooth (CMT) disease strikes 1 in 2500 people. Researchers from the Flanders Interuniversity Institute for Biotechnology (VIB) connected to the University of Antwerp are now demonstrating that mutations in mitofusin 2 are the major cause of CMT2, a specific type of the disease. These findings are important for a better understanding of

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