Associated Papers
Functional characterization of human organic cation transporter OCTN1 single nucleotide polymorphisms in the Japanese population.
Kawasaki Y et al.
Journal of Pharmaceutical Sciences, 2004
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency.
Tang NL et al.
Human Molecular Genetics, 1999
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