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Publications by Steven M. Sine
Mutations Causing Congenital Myasthenia Reveal Principal Coupling Pathway in the Acetylcholine Receptor Ε-Subunit
JCI insight
Medicine
Slow‐channel Myasthenia Due to Novel Mutation in M2 Domain of AChR Delta Subunit
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
Molecular Dissection of Subunit Interfaces in the Acetylcholine Receptor
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Lysine Scanning Mutagenesis Delineates Structural Model of the Nicotinic Receptor Ligand Binding Domain
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
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