Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency
- 16 October 2002
- journal article
- case report
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 77 (3), 195-201
- https://doi.org/10.1016/s1096-7192(02)00169-5
Abstract
No abstract availableKeywords
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