ANXA11 and amyotrophic lateral sclerosis: Reviewing the literature, the spectrum of genotypes and phenotypes associated with ANXA11-related diseases has expanded as follows: (14–26) (i) late-onset or early-onset ALS (black mutations in Figure 2); (ii) ALS with FTD (P36R, G38R, D40Y, D40G, I278V, and G491R); (iii) inclusion body myopathy (hIBM), isolated or in combination with ALS/FTD (D40Y).