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The pore of sodium and potassium channels as a drug receptor.

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Stuehmer,  W.
Department of Membrane Biophysics, MPI for biophysical chemistry, Max Planck Society;

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Stuehmer, W. (1992). The pore of sodium and potassium channels as a drug receptor. Journal of Molecular and Cellular Cardiology, 24(Suppl. Suppl. 5), S116-S116.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0013-0915-8
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