All are genetic amino acid deficiency disease except___________?
A. Phenyl ketonuria
B. Alkaptonuria
C. Homocystinuria
D. 6alactosemia
A. Phenyl ketonuria
B. Alkaptonuria
C. Homocystinuria
D. 6alactosemia
A. Nucleus
B. Lysosomes
C. Mitochondria
D. Golgi apparatus
A. Non Sense mutation of beta chain
B. Missense mutation of beta chain
C. Degradation of beta chain
D. Deletion of beta chain
A. It is a tripetide
B. It converts hemoglobin to methemoglobin
C. It conjugates xenobiotics
D. It scavenges free radicals and superoxide ions
A. Acidic
B. Basic
C. Aromatic
D. Branched chain
A. 5 gm
B. 8 gm
C. 10 gm
D. 16 gm
A. 6
B. 8
C. 12
D. 16
A. Lysine
B. Histidine
C. Tyrosine
D. Proline
A. Protein synthesis
B. Protein degradation
C. Protein denaturation
D. Protein folding
A. 5- Hydroxy indole acetate
B. 3- Hydroxy phenyl pyruvate
C. Phenyl lactate
D. Phenyl acetate