BH4 deficiency identified in a neonatal screening program for hyperphenylalaninemia

Author:

Souza Cezar Antonio Abreu de,Alves Michelle Rosa Andrade,Soares Rosangelis del Lama,Kanufre Viviane de Cássia,Rodrigues Valéria de Melo,Norton Rocksane de Carvalho,Starling Ana Lúcia Pimenta,Aguiar Marcos José Burle de

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference30 articles.

1. Disorders of tetrahydrobiopterin and related biogenic amines;Blau,2001

2. Screening for tetrahydrobiopterin deficiencies using dried blood spots on filter paper;Zurfluh;Mol Genet Metab,2005

3. An international survey of patients with tetrahydrobiopterin deficiencies presenting with hyperphenylalaninaemia;Opladen;J Inherit Metab Dis,2012

4. Treatment of tetrahydrobiopterin deficiencies;Ponzone,2006

5. Characteristics of the hepatic phenylalanine-hydroxylating system in newborn rats;Brenneman;J Biol Chem,1965

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