A. Histidine
B. Cystine
C. Tyrosine
D. Alanine
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Related Mcqs:
- All are genetic amino acid deficiency disease except___________?
- A. Phenyl ketonuria B. Alkaptonuria C. Homocystinuria D. 6alactosemia...
- Which vitamin is related to a co-factor in glycine metabolism is______________?
- A. Vit E B. Folic acid C. Thiamine D. Cobalamine...
- Alkaptonuria, an inherited metabolic disorder of L0tyrosine metabolism is due to lack of_____________?
- A. Parahydroxy phenyl pyruvate Hydroxylase B. Tyrosine transaminase C. Homogentisate oxidase D. Tyrosine oxidase...
- In the body, metabolism of 10 g of protein would produce approximately____________?
- A. 1 Kcal B. 41 Kcal C. 410 Kcal D. 4100 Kcal...
- Incomplete casting is the result of_____________?
- A. More porous investment in the mould B. Narrow sprue diameter C. Hollow sprue pin D. Large reservoir...
- Incomplete fractures of the bone are called___________?
- A. Comminuted fracture B. Compound fracture C. Simple fracture D. Green stick fracture...
- In conn’s disease, there is an excess of______________?
- A. Adrenaline B. Aldosterone C. Cortisol D. Noradrenaline...
- Hansen’s disease is another name of______________?
- A. Leprosy B. Tuberculosis C. Diabetes D. Lichen planus...
- Letterer seiwe disease is a disturbance of______________?
- A. protein metabolism B. histiocytic disorder C. Mucopolysaccharide metabolism D. Carbohydrate metabolism...
- Ketone bodies are by products of metabolism of_____________?
- A. Carbohydrate B. Protein C. Fat D. All of the above...
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