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Phenylketonuria screening in Iranian newborns: a systematic review and meta-analysis

Abstract Background Phenylketonuria (PKU), which is characterized by a deficiency of phenylalanine hydroxylase activity, is an autosomal recessive disorder of phenylalanine (Phe) metabolism. Newborn screening is the main population-based public health screening program that allows successful identif...

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Bibliographic Details
Main Authors: Mehdi Shokri (Author), Parviz Karimi (Author), Hadis Zamanifar (Author), Fatemeh Kazemi (Author), Gholamreza Badfar (Author), Milad Azami (Author)
Format: Book
Published: BMC, 2020-07-01T00:00:00Z.
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