Phenylalanine & Tyrosine Metabolic Disorders
Biochemistry
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Nitrogen Metabolism
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Phenylalanine & Tyrosine
Q. A newborn presents with a mousy-like odor from which enzyme deficiency and syndrome?
a
Fumarylacetoacetate hydrolase/Tyrosinemia
b
Phenylalanine hydroxylase/Phenylketonuria
c
Tyrosine hydroxylase/Tyrosinemia
d
Dihydrobiopterin reductase/Alkaptonuria
e
Homogentisate oxidase/Phenylketonuria
f
Tyrosine hydroxylase/Alkaptonuria
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