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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
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Zuberi S.M., Eunson L.H., Spauschus A., De Silva R., Tolmie J., Wood N.W., et al. A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy. Brain 1999, 122(Pt 5):817-825.
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(1999)
Brain
, vol.122
, pp. 817-825
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Zuberi, S.M.1
Eunson, L.H.2
Spauschus, A.3
De Silva, R.4
Tolmie, J.5
Wood, N.W.6
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