Treatment adherence during childhood in individuals with phenylketonuria: Early signs of treatment discontinuation

Gestores bibliográficos

item.contributor.advisor

ORCID:

Journal Title

Journal ISSN

Volume Title

Publisher

item.page.isbn

item.page.issn

item.page.issne

item.page.doiurl

item.page.extent

item.page.accessRights

item.page.other

item.page.references

Abstract

Introduction: Phenylketonuria (PKU) is an autosomal recessive disorder characterized by a deficiency in phenylalanine (Phe) hydroxylase activity. Early diagnosis and continuous treatment with a low Ph...

Description

item.page.coverage.spatial

item.page.sponsorship

Citation

García, María Ignacia, Gabriela Araya, Soledad Coo, Susan E. Waisbren, and Alicia de la Parra. 2017. “Treatment adherence during childhood in individuals with phenylketonuria: Early signs of treatment discontinuation.” Molecular Genetics and Metabolism Reports 11 (1): 54-58. doi:10.1016/j.ymgmr.2017.04.006. http:// dx.doi.org/10.1016/j.ymgmr.2017.04.006.

item.page.dc.rights

item.page.dc.rights.url

Estadísticas de uso
1 0,8 0,5 0,3 0
Agosto 2025Septiembre 2025Octubre 2025Noviembre 2025Diciembre 2025Enero 2026Febrero 2026