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January 14, 1992Biochemistry

Structural organization and regulatory regions of the human medium-chain acyl-CoA dehydrogenase gene

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Authors

ZZZhifang ZhangCity Of Hope National Medical CenterDaniel P. KellyDaniel P. KellyGeneral CardiologyJKJung Ja Kim

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Zhang et al. (1992) studied this question.

synapsesocial.com/papers/6a97e0c3cb7f2a2edc74cd3bhttps://doi.org/10.1021/bi00116a013
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation.1990 · 102 citations
  2. 2Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.1990 · 90 citations
  3. 3Regulatory regions of the mitochondrial and cytosolic isoenzyme genes participating in the malate-aspartate shuttle.1990 · 27 citations
  4. 4Structural Organization of the Human Mitochondrial Cytochrome c1 Gene1989 · 61 citations