22. Carbamoyl phosphate synthetase I deficiency is an autosomal recessive metabolic disorder that causes __________to accumulate in the blood.
(A) bicarbonate
(B) ammonium
(C)ADP
(D) phosphate
(E) CO2

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統計: A(1), B(3), C(1), D(0), E(0) #2450319

詳解 (共 2 筆)

#4833602

 (B), urea cycle無法進行而導致NH3累積

  • Carbamoyl phosphate synthetase I (mitochondria, urea cycle)
  • Carbamoyl phosphate synthetase II (cytosol, pyrimidine metabolism).
    - ref. wiki


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#5689332
(b)為正解 CPSI 缺乏症是一...
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