Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)
Some researchers even suggest its potential role in skin rejuvenation could quietly replace more invasive cosmetic procedures
[DOI] [PMC free article] [PubMed] [Google Scholar] 53.Widemann B.C., Meyer C.F., Cote G.M., Chugh R., Milhem M.M., Van Tine B.A., Kim A., Turpin B., Dombi E., Jayaprakash N
Tumor cells and tumor-infiltrating myeloid cells have been observed to compete for glutamine uptake via the transporter protein SLC1A5
Cancer research
It also provides you with ongoing support and accountability so you dont slip back into old habits and end up gaining your weight back again