The genetic ailment phenylketonuria (PKU) is The lack to metabolize phenylalanine because of a lack of the enzyme phenylalanine hydroxylase. People today using this dysfunction are often known as "phenylketonurics" and have to regulate their intake of phenylalanine. A (unusual) "variant kind" of phenylketonuria identified as hyperphenylalaninemia is because of https://ericam873cxs5.izrablog.com/profile