Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2 (Q44647365)
scientific article published on January 1, 2003
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Current Data About Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2
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https://onlinelibrary.wiley.com/doi/pdf/10.1023/A%3A1025968502527
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(P1476) "Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2" (language: en)
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"Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2" (language: en)
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(P2093) U. Spiekerkoetter
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G. Huener
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T. Baykal
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M. Demirkol
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M. Duran
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R. Wanders
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J. Nezu
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E. Mayatepek
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other details
description scientific article published on January 1, 2003

External Links
(P356) 10.1023/A:1025968502527
(P698) 14605509
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