Clinical and genetic aspects of Charcot-Marie-Tooth disease subtypes
Soo Hyun Nam, Byung-Ok Choi
Precis Future Med. 2019;3(2):43-68.   Published online 2019 Mar 5     DOI:
Citations to this article as recorded by Crossref logo
Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation
Marzieh Khani, Hanieh Taheri, Hosein Shamshiri, Hamidreza Moazzeni, John Hardy, Jose Tomas Bras, Kolsoum InanlooRahatloo, Afagh Alavi, Shahriar Nafissi, Elahe Elahi
Journal of Neurology.2020;[Epub]     CrossRef