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Mutations in Novel Organic Cation Transporter (OCTN2), an Organic Cation/Carnitine Transporter, with Differential Effects on the Organic Cation Transport Function and the Carnitine Transport Function

Data up to Jan 2025

Published1999
Citations84
References21

Total Citations Per Year

Abstract

References (21)

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1998 • 694 citations

CARNITINE

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Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter

1999 • 540 citations

cDNA Sequence, Transport Function, and Genomic Organization of Human OCTN2, a New Member of the Organic Cation Transporter Family

1998 • 336 citations

Functional characteristics and tissue distribution pattern of organic cation transporter 2 (OCTN2), an organic cation/carnitine transporter.

1999 • 328 citations

Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency

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Molecular Pharmacology of Organic Cation Transporters in Kidney

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Mutations of OCTN2, an Organic Cation/Carnitine Transporter, Lead to Deficient Cellular Carnitine Uptake in Primary Carnitine Deficiency

1999 • 150 citations

Infantile disease with microvesicular fatty infiltration of viscera spontaneously occurring in the C3H-H-2° strain of mouse with similarities to Reye's syndrome

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1984 • 110 citations

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1998 • 103 citations

A Missense Mutation of Mouse OCTN2, a Sodium-Dependent Carnitine Cotransporter, in the Juvenile Visceral Steatosis Mouse

1998 • 84 citations

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