Health, 07.08.2021 04:50, donmak3833
You are studying the DNA of a person who you know has two defective copies of the gene that encodes phenylalanine hydroxylase. However, you also find that this person also carries two defective copies of the gene for homogentisic acid oxidase. (Assume there are no other intermediates available for this pathway.) Will this person exhibit symptoms of both alkaptonuria and phenylketonuria?
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