Treatment adherence during childhood in individuals with phenylketonuria: Early signs of treatment discontinuation
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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...
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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.
Keywords
Adherence , Phenylketonuria , PKU , IQ
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