Cloning and characterization of human ORNT2: a second mitochondrial ornithine transporter that can rescue a defective ORNT1 in patients with the hyperornithinemia–hyperammonemia–homocitrullinuria syndrome, a urea cycle disorder
- 19 July 2003
- journal article
- research article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 79 (4) , 257-271
- https://doi.org/10.1016/s1096-7192(03)00105-7
Abstract
No abstract availableKeywords
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