Publications by authors named "Nghia Trong Tien Hoang"
Brain Behav
September 2022
Article Synopsis
- Charcot-Marie-Tooth (CMT) disease is a common hereditary neuropathy, and identifying mutations is crucial for genetic diagnosis, especially since little genetic data exists for Vietnamese patients.
- The study analyzed 31 Vietnamese CMT patients, finding a 42% mutation detection rate, with PMP22 duplication being the most frequent abnormality and two new mutations identified in the NEFL and PMP22 genes.
- This research highlights the significance of molecular diagnosis in CMT and contributes valuable genetic information for the Vietnamese population affected by the disease.
