IDENTIFICATION OF MUTATIONS IN THE PAH GENE IN PKU PATIENTS IN THE STATE OF MATO GROSSO

OBJECTIVE: To identify phenylalanine hydroxylase (PAH) mutations in patients with phenylketonuria (PKU) from the Newborn Screening Service in Mato Grosso, Midwest Brazil. METHODS: This is a cross-sectional descriptive study. The sample consisted of 19 PKU patients diagnosed by newborn screening. Mol...

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Detalles Bibliográficos
Autores principales: Costa, Roseli Divino, Galera, Bianca Borsatto, Rezende, Bianca Costa, Venâncio, Amanda Cristina, Galera, Marcial Francis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade de Pediatria de São Paulo 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025444/
https://www.ncbi.nlm.nih.gov/pubmed/32074228
http://dx.doi.org/10.1590/1984-0462/2020/38/2018351

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025444/
https://www.ncbi.nlm.nih.gov/pubmed/32074228
http://dx.doi.org/10.1590/1984-0462/2020/38/2018351

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