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All research protocols should follow your institution's guidelines

3.1.5 Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a rare autosomal recessive disease caused by pathogenic variants in the nuclear TYMP gene encoding the thymidine phosphorylase enzyme (Nishino et al., 2000)

CJC-1295 without DAC: Shorter half-life, requires more frequent dosing, but gives more control over timing

if B12 levels were either at the high end of acceptable range, or higher than acceptable range, then the recommendation also included advice to review the frequency of the intervention and to consider changing from 3-monthly interventions to 6-monthly interventions

Thymosin beta4 accelerates wound healing