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[3] Ballatori, N., et al

Pollard JD, Quan T, Li Y, Quan T

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]

Oxidative and nitrative proteinmodifications in Parkinsons disease

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