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OHSU 3 records found Search took 0.14 seconds. 
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Long-chain 3-Hydroxyacyl CoA Dehydrogenase Deficiency (LCHADD) is an autosomal recessive defect in fatty acid oxidation that presents with hypoketotic hypoglycemia and/or [...]
2020 | Abstract |
3.
The overall goal of this project is to conduct a sub-analysis of the primary study data to identify factors related to the magnitude of change from baseline with C7 suppl [...]
2019 | Thesis |

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