Long-term subclinical severe hyperCKemia associated with a rare VPS13A gene mutation in an Iranian patient: Case report

Authors

  • Seyed Jalaleddin Hadei Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran
  • Bardiya Ghaderi-Yazdi Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran
  • Shahriar Nafissi Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran

DOI:

https://doi.org/10.18502/cjn.v23i1.16439

Keywords:

VPS13A Protein Human; Genetic Testing; Chorea-Acanthocytosis; Neuromuscular Disease; Creatine Kinase; Movement Disorders

Abstract

The Article Abstract is not available.

Downloads

Published

2024-09-09

Issue

Volume (23) issue (1)

Section

Articles