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SEPT9 happens to be connected to various intracellular features, such as for instance cytokinesis and membrane layer trafficking. Interestingly, SEPT9-mutations are recognized to cause hereditary neuralgic amyotrophy (HNA), a recurrent focal peripheral neuropathy. SUMMARY We, the very first time, provide a SEPT9 variant associated to a CMT phenotype and advise SEPT9 as brand-new sufficient applicant gene in CMT.BACKGROUND Danhong shot (DHI), that will be one of

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