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  • Novel mutations in the Na+,... Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions
    Vanmolkot, Kaate R. J.; Kors, Esther E.; Hottenga, Jouke-Jan ... Annals of neurology, September 2003, Letnik: 54, Številka: 3
    Journal Article
    Recenzirano

    Familial hemiplegic migraine (FHM) is a rare, severe, autosomal dominant subtype of migraine with aura. Up to 75% of FHM families have a mutation in the P/Q‐type calcium channel Cav2.1 subunit ...
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