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
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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