Autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation
MONDO:0044625Also known as: CMT2 due to DGAT2 mutation
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials
Also known as: CMT2 due to DGAT2 mutation
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials