Among the various subtypes of CMT, CMT1A is the most common form, characterized by a duplication of the PMP22 gene. Despite being a well-known genetic abnormality associated with CMT1A ...

The study enrolled CMT1A patients, whose disease was caused by a mutation in the PMP22 gene on chromosome 17. The Paris-based company said that the trial was scuppered by a high placebo response ...

International cooperation project launched under the joint leadership of the University Medical Center Göttingen (UMG) and the Timone University Hospital in Marseille, France, to identify new ...