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Inborn Errors of Metabolism program – application form A

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Publication date: 
2 September 2019
Last updated: 
3 March 2020
Publication type: 
Form
Intended audience: 
General public
Description: 

This application form is for individuals diagnosed with dihydropteridine reductase (DHPR) deficiency, hyperphenylalaninemia or phenylketonuria (PKU). Individuals with these conditions must be reassessed and reapply for the program every 12 months.