RS137960129 MFN2
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Associated Conditions
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Inborn genetic diseases
Hereditary motor and sensory neuropathy with optic atrophy
Charcot-Marie-Tooth disease type 2
Charcot-Marie-Tooth disease
Inborn genetic diseases
Other Variants in MFN2