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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
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https://hal-riip.archives-ouvertes.fr/pasteur-01469443
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Submitted on : Thursday, February 16, 2017 - 2:40:55 PM
Last modification on : Wednesday, October 28, 2020 - 9:52:04 AM

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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, SAGE Publications (UK and US), 2016, 31 (7), pp.843--849. ⟨10.1177/0883073815623636⟩. ⟨pasteur-01469443⟩

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