Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients

Author:

Khatami Shohreh,Dehnabeh Soghra Rouhi,Zeinali Sirous,Thöny Beat,Alaei Mohammadreza,Salehpour Shadab,Setoodeh Aria,Rohani Farzaneh,Hajivalizadeh Fatemeh,Samavat Ashraf

Publisher

Springer Berlin Heidelberg

Reference11 articles.

1. Arai N, Narisawa K, Hayakawa H et al (1982) Hyperphenylalaninemia due to dihydropteridine reductase deficiency: diagnosis by enzyme assays on dried blood spots. Pediatrics 70:426–430

2. Atherton ND (1989) HPLC measurement of phenylalanine by direct injection of plasma onto an internal-surface reversed-phase silica support. Clin Chem 35(6):975–978

3. BIOMDB: Database of Mutations Causing Tetrahydrobiopterin Deficiencies (database online) ( http://www.biopku.org/BioPKU_DatabasesBIOMDB.asp ) curated by N. Blau, B. Thöny

4. Blau N, Thöny B, Cotton RGH (2001) Disorders of tetrahydrobiopterin and related biogenic amines. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Vogelstein B (eds) The metabolic and molecular bases of inherited disease, 8th edn. McGraw-Hill, New York, pp 1725–1776

5. Blau N, Duran M, Gibson KM (2008) Laboratory guide to the methods in biochemical genetics techniques. Springer, Heidelberg, pp 696–699

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