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Rare mutations in SLC22A5 can cause hypoglycemia and liver problems from infancy, and this is one of the genetic conditions that is usually screened for at birth
(2019) A randomized, double-blinded, placebo-controlled, parallel trial of vitamin D3 supplementation in adult patients with migraine
Rare cases of muscle weakness or cramps
Induction of apoptosis by L-carnitine through regulation of two main pathways in Hepa1c1c 7 cells
