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1. Introduction The ability of humans to transport themselves throughout their environment is a critical component of an untold number of goal-directed activities essential to the survival of the species. Many individuals with genetic mutations resulting in developmental disorders have difficulty walking in an efficient and effective manner.
1. Introduction NGLY1 Deficiency is an autosomal recessive congenital disorder identified in less than 100 individuals by 2022 [1] . One instance of NGLY1 Deficiency was described in 2012, with several variants of this condition being described since [2] . However, there are similar characteristics among the variants.
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