The Unique α4(+)/(−)α4 Agonist Binding Site in (α4)3(β2)2 Subtype Nicotinic Acetylcholine Receptors Permits Differential Agonist Desensitization Pharmacology versus the (α4)2(β2)3 Subtype
Data Supplement
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Supplemental Figure - Figure S1: Mutation of the putative alpha4(+)/(-)alpha4 agonist binding pocket.