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Results 1 - 4 of 4 for "Migraine," familial "hemiplegic," 2
  1. ATP1A2 gene 
    ... ATP1A2 gene have been identified in people with familial hemiplegic migraine type 2 (FHM2). This condition is characterized by migraine headaches ... 0000127310.11526.fd. Citation on PubMed Pietrobon D. Familial hemiplegic migraine. Neurotherapeutics. 2007 Apr;4(2):274-84. doi: 10.1016/j.nurt.2007. ...
    https://medlineplus.gov/genetics/gene/atp1a2 - Genetics
  2. CACNA1A gene 
    ... Luvisetto S, Striessnig J, Fletcher C, Pietrobon D. Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  3. SCN1A gene 
    ... 1002/humu.20178. Citation on PubMed Pietrobon D. Familial hemiplegic migraine. Neurotherapeutics. 2007 Apr;4(2):274-84. doi: 10.1016/j.nurt.2007. ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  4. PRRT2 gene 
    ... begin in infancy and usually disappear by age 2. ICCA is characterized by both ... hemiplegic migraine (described above) can also cause BFIS and ICCA. ...
    https://medlineplus.gov/genetics/gene/prrt2 - Genetics