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organic cation transporter octn2
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A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic…
Analysis of blood carnitine profile and SLC22A5 gene variants in 17 neonates with Primary carnitine …
Newborn screening for primary carnitine deficiency: who will benefit? - a retrospective cohort study…
Identification of variants in genes associated with hypertrophic cardiomyopathy in Mexican patients.
Screening of 1.17 million newborns for inborn errors of metabolism using tandem mass spectrometry in…
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Influence of OCTN2 Variants on Carnitine Status and Plasma Triglycerides
Clinical Evidence of pH Dependent ß2 Adrenergic Transport Mechanisms in the Airway
Influence of Intestinal Transporter Genetic Variants on the Bioavailability of Gabapentin
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