LRP4 and myasthenia gravis: Myasthenia gravis (MG) is an autoimmune neuromuscular disease characterized by fluctuating musculoskeletal weakness, commonly caused by antibodies against acetylcholine receptors (AChRs), muscle-specific kinase (MuSK), or anti-low-density lipoprotein receptor-related protein 4 (LRP4) at the neuromuscular junctions [1,2].