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phenylketonuria; mutation; frequency; PCR/RFLP assays.

Sameh Khemir¹ Hajer Siala² Sameh Hadj Taieb¹ Wafa Cherif³ Hatem Azzouz⁴ Rym Kéfi³ Sonia Abdelhak³ Naziha Khouja⁵ Neji Tebib⁴ Taieb Massaoud² Marie Françoise Ben Dridi⁴ Naziha Kaabachi⁶

1. Laboratory of Biochemistry, Department of Paediatrics, Rabta Hospital, 1007 Jebbari, Tunis, Tunisia
2. Laboratory of Biochemistry and Molecular Biology, Children’s Hospital, 1007 Jebbari, Tunis, Tunisia
3. Research Unit UR04/SP03, Pasteur Institute, 1002 Tunis-Belvedere, Tunis, Tunisia
4. Department of Paediatrics, Rabta Hospital, 1007 Jebbari, Tunis, Tunisia
5. Department of Paediatrics, Neurology Institute, 1007 Jebbari, Tunis, Tunisia
6. Laboratory of Biochemistry, Rabta Hospital, 1007 Jebbari, Tunis, Tunisia

Published

April 2011

Manuscript received

4 November 2010

Manuscript revised

9 August 2011

Accepted

22 November 2011

Early published

16 March 2012