Nature Genetics
37, 733 - 738 (2005)
Published online: 5 June 2005; | doi:10.1038/ng1585
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorderWei Du, Jocelyn F Bautista, Huanghe Yang, Ana Diez-Sampedro, Sun-Ah You, Lejin Wang, Prakash Kotagal, Hans O Lüders, Jingyi Shi, Jianmin Cui, George B Richerson
& Qing K WangSupplementary Fig. 1 (pdf 108K)
KCNMA1 mutation D434G co-segregates with GEPD patients in the family.
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