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Taken together, the progressive elucidation and investigation of ALS-related disease-causing genes, the successful construction of disease models through the utilization of technologies such as exon sequencing and gene editing, and the further investigation of the potential molecular regulatory mechanisms between ALS mutant genes and mitochondria will facilitate the opening of a new avenue for the study of targeted therapy for ALS disease

Head-to-head structural and pharmacological comparisons with other emerging long-acting amylin analogs are an anticipated direction as additional compounds in the class advance