Targeted next generation sequencing identifies a genetic spectrum of DNA variants in patients with hemiplegic migraine

• 主要な著者: Neven Maksemous (著者), Robert A Smith (著者), Heidi G Sutherland (著者), Bridget H Maher (著者), Omar Ibrahim (著者), Garth A Nicholson (著者), Elisabeth P Carpenter (著者), Rod A Lea (著者), M Zameel Cader (著者), Lyn R Griffiths (著者)
• フォーマット: 図書
• 出版事項: SAGE Publishing, 2019-10-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

Objective: Hemiplegic migraine in both familial (FHM) and sporadic (SHM) forms is a rare subtype of migraine with aura that can be traced to mutations in the CACNA1A , ATP1A2 and SCN1A genes. It is characterised by severe attacks of typical migraine accompanied by hemiparesis, as well as episodes of...