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Familial epilepsy in Algeria: Clinical features and inheritance profiles |
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Published in | Seizure. 2015, vol. 31, p. 12-18 | |
Abstract | To document the clinical characteristics and inheritance pattern of epilepsy in multigeneration Algerian families. | |
Identifiers | PMID: 26362371 | |
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Research group | Pathologie Moléculaire de la Trisomie 21 et le Génome Humain (248) | |
Citation (ISO format) | CHENTOUF, Amina et al. Familial epilepsy in Algeria: Clinical features and inheritance profiles. In: Seizure, 2015, vol. 31, p. 12-18. doi: 10.1016/j.seizure.2015.06.015 https://archive-ouverte.unige.ch/unige:77405 |