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Publications by Xin‐Ming Shen
Slow‐channel Myasthenia Due to Novel Mutation in M2 Domain of AChR Delta Subunit
Annals of Clinical and Translational Neurology
Neuroscience
Neurology
Related publications
Liddle’s Syndrome in an African Male Due to a Novel Frameshift Mutation in the Beta-Subunit of the Epithelial Sodium Channel Gene
Cardiovascular Journal of Africa
Medicine
Cardiovascular Medicine
Cardiology
Recombinant Expression of the AChR-alpha1 Subunit for the Detection of Conformation-Dependent Epitopes in Myasthenia Gravis
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
Core-Rod Myopathy Due to a Novel Mutation in BTB/POZ Domain of KBTBD13 Manifesting as Late Onset LGMD
Acta neuropathologica communications
Forensic Medicine
Molecular Neuroscience
Pathology
Neurology
Cellular
The Human Δ1261 Mutation of theHERGPotassium Channel Results in a Truncated Protein That Contains a Subunit Interaction Domain and Decreases the Channel Expression
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Recurrent Hyperparathyroidism Due to a Novel CDC73 Splice Mutation
Journal of Bone and Mineral Research
Endocrinology
Orthopedics
Sports Medicine
Metabolism
Diabetes
Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene
American Journal of Human Genetics
Genetics
Juvenile Onset Autoinflammatory Disease Due to a Novel Mutation in TNFAIP3 (A20)
Arthritis Research & Therapy
M2 Delta, a Candidate for the Structure Lining the Ionic Channel of the Nicotinic Cholinergic Receptor.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Congenital Long-Qt Syndrome Caused by a Novel Mutation in a Conserved Acidic Domain of the Cardiac Na+ Channel
Circulation
Cardiovascular Medicine
Physiology
Cardiology
