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

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 identification...

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Detalles Bibliográficos
Autores principales:	Shokri, Mehdi, Karimi, Parviz, Zamanifar, Hadis, Kazemi, Fatemeh, Badfar, Gholamreza, Azami, Milad
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2020
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379797/ https://www.ncbi.nlm.nih.gov/pubmed/32703178 http://dx.doi.org/10.1186/s12887-020-02230-6

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