Fig. 1From: Directly converted patient-specific induced neurons mirror the neuropathology of FUS with disrupted nuclear localization in amyotrophic lateral sclerosisSchematic diagram of functional domains of the FUS protein with gene mutations identified in patients with ALS are provided. All three patients enrolled in this study have FUS mutations (p.G504Wfs*12, p.R495*, p.Q519E) that affect the NLS region. Q/G/S/Y rich = Gln/Gly/Ser/Tyr-rich domain; RGG = Arg/Gly/Gly-rich motifs; E = nuclear export signal; RRM = RNA-recognition motif; ZnF = zinc-finger motif; L = nuclear localization signalBack to article page