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Biochemistry Amino Acid Metabolic Disorder 566e8fa6

Hartnup disease, limiting amino acid -

A
Tyrosine
B
Tryptophan
C
Phenylalanine
D
None
High-Yield Explanation
Ans is 'b' i. e., Tryptophan Co-Factor/Limiting Amino Acid Therapy CofactorLimiting amino acido PKU-Tyrosineo Neonatal tyrosinemia. Alkaptonuria, HawkinsuriaVit.C-o Maple Syrup Urine diseaseB1 (Thiamine)-o Hartnup diseaseNiacinTryptophano Mitochondrial diseaseB6-o Classical HomocystinuriaB6 & Folic a.Cystineo Methyl Malonyl acidemiaB12 o Isovaleric acidemia-Glycine, carnitine

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