Title : The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.

Pub. Date : 2009 Jul

PMID : 19287344






1 Functional Relationships(s)
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1 These results suggest a potential physiologic role for the SLC25A29 transporter in the oxidation of fatty acids, ornithine degradation pathway, and possibly the urea cycle. Fatty Acids solute carrier family 25 member 29 Homo sapiens