Xin‐Ming Shen

Rapsyn Mutations in Humans Cause Endplate Acetylcholine-Receptor Deficiency and Myasthenic Syndrome

Kinji Ohno, Andrew G. Engel, Xin‐Ming Shen et al. · The American Journal of Human Genetics · 2002 · 237 citations · Full text

Mendelian Disorder, Rapsyn Mutations, Medicine +9

Myasthenic syndrome caused by mutation of the <i>SCN4A</i> sodium channel

Akira Tsujino, Chantal Maertens, Kinji Ohno et al. · Proceedings of the National Academy of Sciences · 2003 · 175 citations · Full text

Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability

Xin‐Ming Shen, Duygu Selcen, Joan M. Brengman et al. · Neurology · 2014 · 125 citations · Full text

Dok‐7 myasthenia: Phenotypic and molecular genetic studies in 16 patients

Duygu Selcen, Margherita Milone, Xin‐Ming Shen et al. · Annals of Neurology · 2008 · 123 citations · Full text

The spectrum of mutations causing end-plate acetylcholinesterase deficiency

Kinji Ohno, Andrew G. Engel, Joan M. Brengman et al. · Annals of Neurology · 2000 · 120 citations