Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2 (Q44647365)
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scientific article published on January 1, 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2 |
scientific article published on January 1, 2003 |
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Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2 (English)
1 reference
Silent and symptomatic primary carnitine deficiency within the same family due to identical mutations in the organic cation/carnitine transporter OCTN2 (English)
1 reference
U. Spiekerkoetter
G. Huener
T. Baykal
M. Demirkol
M. Duran
R. Wanders
J. Nezu
1 January 2003
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Identifiers
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