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

Internet

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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