Incidence of phenylketonuria (PKU) in Iran
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF02752654.pdf
Reference14 articles.
1. FoilingA: Ueber Ausscheidung von Pheylbrenztraubens aeure in den Harn als Stoffwechsel anomalie in Verbindung mit Imbezillitaet. Hoppe-Seylers Z Physiol Chem 227: 169, 1934
2. Kaufman S: A new cofactor required for the enzymatic conversion of phenylalanine to tyrosine. J Biol Chem 230: 931, 1958
3. Jervis GA: The genetics of Phenylpyruvic oligophrenia. J Ment Sci 85: 719, 1939
4. Woolf LI, Goodwin BL, Cranstou WI, Wade DN, Woolf F, Hadson FP, and McBean MS: A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninemia) Lancet 1: 114, 1968
5. Lenz W; Medizinische Geneti, 4th Edition, G. Thieme Verlang Stuttgart. P 187, 1979
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