A novel mutation in the ATP1A2 gene associated with a sporadic hemiplegic migraine and multiple supraventricular arrhythmias: A case report

• Main Authors: Sarvnaz Shalchian Tehran (Author), Pierre Maquet (Author)
• Format: Knjiga
• Izdano: SAGE Publishing, 2024-10-01T00:00:00Z.
• Teme: article
• Online dostop: Connect to this object online.

Introduction ATP1A2 mutations are identified as a genetic cause of type 2 hemiplegic migraine, but to date, no ATP1A2 gene variant has been linked to heart rhythm disorders Case presentation A 37-year-old woman presented with sporadic hemiplegic migraine and multiple supraventricular arrhythmias ref...