First case report of Charcot-Marie-Tooth disease type 2CC with a frameshift mutation of NEFH gene in Greece

Neurol Sci. 2021 Oct;42(10):4377-4379. doi: 10.1007/s10072-021-05402-z. Epub 2021 Jul 18.

Authors

Andriana Charalampopoulou¹, Dimitra Veltsista², Stavros Taraviras¹, Elisabeth Chroni³

Affiliations

¹ Department of Physiology, School of Medicine, University of Patras, 26504, Patras, Greece.
² Department of Neurology, School of Medicine, University of Patras, 26504, Patras, Greece.
³ Department of Neurology, School of Medicine, University of Patras, 26504, Patras, Greece. echroni@yahoo.com.

PMID: 34275023
DOI: 10.1007/s10072-021-05402-z

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Charcot-Marie-Tooth Disease* / genetics
Frameshift Mutation
Greece
Humans
Mutation
Neurofilament Proteins

Substances

Neurofilament Proteins