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56 A lethal case of HK deficiency was found to be due to an intragenic deletion of 9.5 kb, causing the deletion of exons 5 to 8 of HK1, resulting in a null allele
cocomo-skin-step6-variant:45366437511414
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Both SPMS and PPMS patients show comparable lesion activity and no differences in lesion pathology [26]
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