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

نویسندگان
doi
10.18502/cjn.v23i1.16439
چکیده

کلیدواژه‌ها
Seyed Jalaleddin Hadei1, Bardiya Ghaderi-Yazdi1, Shahriar Nafissi2, VPS13A Protein Human, Genetic Testing, Chorea-Acanthocytosis, Neuromuscular Disease, Creatine Kinase, Movement Disorders