Suppose a human metabolic disease only allows electrons to be used from NADH and not FADH2. What is a probable cause of this disease?
A) a defect in assembly protein genes for complex II of the electron transfer system
B) enzyme defects in glycolysis and the citric acid cycle
C) a deficient amount of cytochrome c and coenzyme Q
D) improper regulation of phosphofructokinase
E) inability of oxygen to act as a final electron acceptor
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