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Publications by Peter N. Robinson
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal Γ Subunit
American Journal of Human Genetics
Genetics
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Fetal Acetylcholine Receptor Inactivation Syndrome
Neurology: Neuroimmunology and NeuroInflammation
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Mutations Causing Congenital Myasthenia Reveal Principal Coupling Pathway in the Acetylcholine Receptor Ε-Subunit
JCI insight
Medicine
Involvement of Human Muscle Acetylcholine Receptor Alpha-Subunit Gene (CHRNA) in Susceptibility to Myasthenia Gravis.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Postsynaptic Development of the Neuromuscular Junction in Mice Lacking the Γ-Subunit of Muscle Nicotinic Acetylcholine Receptor
Journal of Molecular Neuroscience
Medicine
Molecular Neuroscience
Cellular
Acetylcholine Receptor-Inducing Activity Stimulates Expression of the Epsilon-Subunit Gene of the Muscle Acetylcholine Receptor.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Noninvasive Prenatal Diagnosis of a Fetal Microdeletion Syndrome
New England Journal of Medicine
Medicine
Molecular Dissection of Subunit Interfaces in the Acetylcholine Receptor
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Acetylcholine Receptor Δ Subunit Mutations Underlie a Fast-Channel Myasthenic Syndrome and Arthrogryposis Multiplex Congenita
Journal of Clinical Investigation
Medicine
A Juxta-Membrane Epitope on the Human Acetylcholine Receptor Recognized by T Cells in Myasthenia Gravis.
Journal of Clinical Investigation
Medicine