MG patients are classified according to a combination of features: age of onset, i.e., early-onset (EOMG) and late-onset MG (LOMG); the affected muscle district, i.e., ocular (if symptoms remain confined to this region for at least 2 years), axial, limb, or bulbar; presence of specific auto-antibodies, i.e., mainly anti-acetyl-choline receptor (AchR, the most common), anti-muscle-specific kinase (MuSK), and anti-lipoprotein receptor-related peptide 4 (LRP4), abnormalities of the thymus (e.g., hyperplasia, thymoma), and other autoimmune disorders [3]. Here, LRP4 is linked to myasthenia gravis.