The defect in a slow channel myasthenic syndrome mutant, epsilon L221F

The defect in a slow channel myasthenic syndrome mutant, epsilon L221F

Podrobná bibliografie
Hlavní autoři:	Hatton, C, Chen, J, Shelley, C, Croxen, R, Beeson, D, Colquhoun, D
Médium:	Journal article
Vydáno:	2000

Podobné jednotky

Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.
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