O-176 New Tunisian Mutation In Pyridoxine – Dependent Epilepsy

N Hentati; A Ben Thabet; A Tlili; L Walha; R Regaieg; A Bouraoui; A Gargouri

doi:10.1136/archdischild-2014-307384.244

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Headache and Genetics

O-176 New Tunisian Mutation In Pyridoxine – Dependent Epilepsy

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N Hentati 1Neonatology, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles
A Ben Thabet 1Neonatology, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles
A Tlili 2Laboratory of Molecular Human Genetics Faculty of Medicine, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles
L Walha 1Neonatology, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles
R Regaieg 1Neonatology, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles
A Bouraoui 1Neonatology, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles
A Gargouri 1Neonatology, CHU Hédi Chaker Sfax Tunisia, Sfax, Tunisia PubMed articles Google scholar articles

Citation

Hentati N, Ben Thabet A, Tlili A, et al

O-176 New Tunisian Mutation In Pyridoxine – Dependent Epilepsy

Archives of Disease in Childhood 2014;99:A92.

Publication history

First published October 14, 2014.

Online issue publication

July 09, 2018

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