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

  • 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.

Published
2024-09-09
Issue
Volume (23) issue (1)
Section
Articles