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[DOI] [PubMed] [Google Scholar] 256.Miserocchi G, Sancini G, Mantegazza F, Chiappino G

Loss-of-function mutations in the BCKDK gene are associated with a phenotype that is characterized by persistently reduced levels of BCAA in body fluids, developmental delay, microcephaly, and neurobehavioral abnormalities

Food raises insulin, and elevated insulin significantly blunts GH release

Progress in the identification of these pathways is slow due to the lack of a thorough understanding of these complex neuroprotective signaling pathways

It will ensure theres enough B12 in the blood to replenish the cells and tissues around the clock, and cure the deficiency