Japanese cases of familial hemiplegic migraine with cerebellar ataxia carrying a T666M mutation in the CACNA1A gene

Lignende værker

• Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
  af: Ducros, A, et al.
  Udgivet: (1999)
• Familial Hemiplegic Migraine With Progressive Cerebellar Ataxia Caused by a p.Thr666Met CACNA1A Gene Mutation in a Chinese Family
  af: Mengmeng Li, et al.
  Udgivet: (2019-11-01)
• Familial Hemiplegic Migraine With Progressive Cerebellar Ataxia Caused by a p.Thr666Met CACNA1A Gene Mutation in a Chinese Family
  af: Li, Mengmeng, et al.
  Udgivet: (2019)
• Familial Hemiplegic Migraine with Prolonged Coma and Cerebellar Atrophy: CACNA1A T666M Mutation in a Korean Family
  af: Choi, Kyung-Ho, et al.
  Udgivet: (2012)
• Migraine and Cerebellar Ataxia
  af: J Gordon Millichap
  Udgivet: (1990-09-01)