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The defect in a slow channel m...
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The defect in a slow channel myasthenic syndrome mutant, epsilon L221F
Bibliografske podrobnosti
Main Authors:
Hatton, C
,
Chen, J
,
Shelley, C
,
Croxen, R
,
Beeson, D
,
Colquhoun, D
Format:
Journal article
Izdano:
2000
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Opis
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Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.
od: Hatton, C, et al.
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Effects of epsilon L78P, an acetylcholine receptor mutation that causes slow channel congenital myasthenic syndrome.
od: Shelley, C, et al.
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Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
od: Croxen, R, et al.
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Recessive inheritance and variable pentrance of slow channel myasthenic syndromes
od: Besson, D, et al.
Izdano: (2002)
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes (Retracted Article. See vol 72, pg 294, 2009)
od: Croxen, R, et al.
Izdano: (2002)