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» MYO9B gene mutations tied to CMT2 and optic atrophy, study finds
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MYO9B gene mutations tied to CMT2 and optic atrophy, study finds
May 31, 2023
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Charcot-Marie-Tooth disease (CMT) is a group of neuropathies characterized by sensory and motor dysfunction that progress with aging. It is considered that about 60% of the axonal forms of the disease, such as CMT2, remain genetically undiagnosed.
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