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Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)
James SJ, Cutler P, Melnyk S, Jernigan S, Janak L, Gaylor DW et al
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The improvements by liraglutide treatment were relatively modest, though the effect is superior to the effects of antibody-type drugs that are on the market [197]
Can help in promoting the immune system, thus improving the body's defence system
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