Coriell Institute for Medical Research

Publication

Kaunisto MA, Harno H, Vanmolkot KR, Gargus JJ, Sun G, Hämäläinen E, Liukkonen E, Kallela M, van den Maagdenberg AM, Frants RR, Färkkilä M, Palotie A, Wessman M, A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2 Neurogenetics5:141-6 2004
PubMed ID: 15133718

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