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

Author(s):

Seyed Jalaleddin Hadei , Bardiya Ghaderi-Yazdi , Shahriar Nafissi *

Message:
Article Type:
Editorial (دارای رتبه معتبر)
Keywords:

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

Language:
English
Published:
Current Journal of Neurology, Volume:23 Issue: 1, Winter 2024
Pages:
86 to 88
https://www.magiran.com/p2775933  
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