however, the only statistically significant difference was between the LD control group and both groups switched from WD to LD, regardless of their treatment (Supplementary Fig
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Preclinical models used oral dosing at 50100mg/kg body weight, but human-equivalent subcutaneous protocols typically range from 30mg to 50mg per injection, administered once daily
Its fast-acting injectable form makes it especially useful in managing neuropathy, severe deficiencies, and conditions where oral supplementation is not feasible, supporting faster recovery and improved neurological well-being
