Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.

Specchio, Nicola; Marini, Carla; Terracciano, Alessandra; Mei, Davide; Trivisano, Marina; Sicca, Federico; Fusco, Lucia; Cusmai, Raffaella; Darra, Francesca; Bernardina, Bernardo Dalla; Bertini, Enrico; Guerrini, Renzo; Vigevano, Federico

Specchio, Nicola; Marini, Carla; Terracciano, Alessandra; Mei, Davide; Trivisano, Marina; Sicca, Federico; Fusco, Lucia; Cusmai, Raffaella; Darra, Francesca; Bernardina, Bernardo Dalla; Bertini, Enrico; Guerrini, Renzo; Vigevano, Federico.

Affiliation

Specchio N; Neurology Unit, Department of Neuroscience, Bambino Gesu' Children's Hospital-IRCCS, Piazza S. Onofrio 4, Rome, Italy. nicola.specchio@opbg.net

Epilepsia ; 52(7): 1251-7, 2011 Jul.

Article in En | MEDLINE | ID: mdl-21480887

Subject(s)

Cadherins/genetics; Epilepsy/genetics; Age of Onset; Brain/physiopathology; Child, Preschool; Electroencephalography; Epilepsy/physiopathology; Female; Frameshift Mutation/genetics; Humans; Infant; Mutation, Missense/genetics; Phenotype; Protocadherins; Seizures/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cadherins / Epilepsy Limits: Child, preschool / Female / Humans / Infant Language: En Journal: Epilepsia Year: 2011 Type: Article Affiliation country: Italy

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