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September 1, 2001Human Molecular GeneticsOpen Access

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse

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KCKeith B. CoxUniversity of Alabama at Birmingham

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Keith B. Cox (2001) studied this question.

synapsesocial.com/papers/6a9e57e4c448d60cdc3683f5https://doi.org/10.1093/hmg/10.19.2069
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Purification and characterization of short-chain, medium-chain, and long-chain acyl-CoA dehydrogenases from rat liver mitochondria. Isolation of the holo- and apoenzymes and conversion of the apoenzyme to the holoenzyme.1985 · 220 citations
  2. 2Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients.1995 · 164 citations
  3. 3Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase.1992 · 246 citations