Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the a

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Date: 2011-11-10 05:39:05 Medicine Biology Pediatrics PKU Phenylalanine Newborn screening Dominance Tetrahydrobiopterin deficiency Hyperphenylalanemia Health Mental retardation Phenylketonuria		Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the a Add to Reading List Source URL: www.maine.gov Download Document from Source Website File Size: 22,36 KB Share Document on Facebook

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