Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects

Sameh Khemir (1) , Soumaya Halayem (2, 3) , Hatem Azzouz (4) , Hajer Siala (5) , Maherzia Ferchichi (4) , Asma Guedria (6) , Amel Bedoui (4) , Sonia Abdelhak (7) , Taïeb Messaoud (5) , Neji Tebib (4) , Ahlem Belhaj (6, 2) , Naziha Kaabachi (1)

1 Research Laboratory LR99ES11, Department of Biochemistry, Rabta Hospital, Faculty of Medicine of Tunis
2 Faculty of Medicine of Tunis
3 Department of Child Psychiatry
4 Département de Pédiatrie, Unité des maladies métaboliques héréditaires
5 Laboratory of Biochemistry and Molecular Biology, Tunis
6 Department of Child Psychiatry, La Marsa
7 Institut Pasteur de Tunis

Domaines: Sciences du Vivant [q-bio]

Sameh Khemir, Soumaya Halayem, Hatem Azzouz, Hajer Siala, Maherzia Ferchichi, et al.. Autism in Phenylketonuria Patients: From Clinical Presentation to Molecular Defects . Journal of Child Neurology, 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩. ⟨pasteur-01469443⟩