Molecular architecture of acetylcholinesterase collagen‐tailed forms; construction of a glycolipid‐tailed tetramer.Nathalie Duval, S. Bon, Françoise Coussen et al.|The EMBO Journal|1992Cited by 46
Patients with congenital myasthenia associated with end-plate acetylcholinesterase deficiency show normal sequence, mRNA splicing, and assembly of catalytic subunits.Shelley Camp, Palmer Taylor, S. Bon et al.|Journal of Clinical Investigation|1995Cited by 22
THE POLYMORPHISM OF CHOLINESTERASES: Classification of molecular forms; Interactions and solubilization characteristics; Metabolic relationships and regulationsJean Massoulié, Marc Vigny, Moshé Lazar et al.|Unknown|1984Cited by 21
Mutations in the Catalytic Subunit of Acetylcholinesterase do not Appear Responsible for Congenital Myasthenic Syndrome Associated with End-Plate Acetylcholinesterase DeficiencyShelley Camp, Palmer Taylor, Jean Massoulié et al.|Unknown|1995Cited by 0