Missense mutations of DCTN1, the gene encoding p150Glued, have been linked to different neurodegenerative diseases, in which the G59S missense mutation was linked to autosomal dominant motor neuron disease, and 13 more mutations (F52L, K56R, G67D, K68E, G71A/R/E/V, T72P, Q74P, Y78C/H, and Q93H) were associated with Perry syndrome[5–8]. Here, DCTN1 is linked to Perry syndrome.