Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation
MONDO:0018567Also known as: CMT2 due to TFG mutation
9 clinical trials for this condition and its sub-types.
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Also known as: CMT2 due to TFG mutation
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials