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Carnitine transporter mutations in Crohn's disease consists of missense mutation(s) in the gene coding plasma membrane transporter OCTN1 (SLC22A4) and/or mutation(s) in the promoter of the gene encoding OCTN2 (SLC22A5) [14, 35]
Human aging, muscle mass, and fiber type composition
Somerset Therapeutics Cyanocobalamin for injection 1000 mcg Multiple-Dose Vials 30 mL
I have basically sensitive skin, but it doesn't irritate it
Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels
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