SAGE Reference - Encyclopedia of Global Health

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Phenylketonuria

By: John Michael Quinn V.
In: Encyclopedia of Global Health
Edited by: Yawei Zhang
Subject:Public Health (general), Public Health Education & Health Promotion
Keywords:access to care; genes; genetic disorders; mental retardation; mutation; phenylketonuria; prognosis

Phenylketonuria (PKU) is an inherited genetic disorder that increases blood levels of the essential amino acid phenylalanine (a building block of protein). It is normally obtained through the diet in regulated levels. If PKU is not treated, excess phenylalanine can build ...

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  V., J. (2008). Phenylketonuria. In Y. Zhang (Ed.), Encyclopedia of global health (Vol. 1, pp. 1375-1375). SAGE Publications, Inc., https://www.doi.org/10.4135/9781412963855.n968
  
  V., John Michael Quinn. "Phenylketonuria." In Encyclopedia of Global Health, edited by Zhang, Yawei, 1375-1375. Thousand Oaks, CA: SAGE Publications, Inc., 2008. http://dx.doi.org/10.4135/9781412963855.n968.
  
  V., J. 2008. Phenylketonuria. In: Yawei Zhang Editor, 2008. Encyclopedia of Global Health, Thousand Oaks, CA: SAGE Publications, Inc. pp. 1375 Available at: <http://www.doi.org/10.4135/9781412963855.n968> [Accessed 19 Apr 2021].
  
  V., John Michael Quinn. "Phenylketonuria." Encyclopedia of Global Health. Edited by Yawei Zhang. Vol. 1. Thousand Oaks: SAGE Publications, Inc., 2008, pp. 1375-1375. SAGE Knowledge. 19 Apr 2021, doi: http://www.doi.org/10.4135/9781412963855.n968.
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