Associated Papers
Genetic Heterogeneity of SLC22 Family of Transporters in Drug Disposition.
Lozano E et al.
Journal of Personalized Medicine, 2018
OCTN1 variant L503F is associated with familial and sporadic inflammatory bowel disease.
Lin Z et al.
Journal of Crohn's & Colitis, 2010
Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4).
Urban TJ et al.
Pharmacogenetics and Genomics, 2007
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