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Phenylketonuria, the genetic disorder causing an inborn error of metabolism is an example of
Option: 1
Autosomal dominant
Option: 2
Autosomal recessive
Option: 3
X-linked dominant
Option: 4
X-linked recessive
Answers (1)
As already discussed in Phenylketonuria -
- It is an inborn error of metabolism, which is inherited as an autosomal recessive trait.
- It is a rare disease in which the individual is born without the ability to properly breakdown an amino acid called phenylalanine.
- Hence, the correct option is (b).
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