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Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy.
Gursoy, Semra; Ataman, Esra; Baysal, Bahar Toklu; Özyilmaz, Berk; Gençpinar, Pinar; Hiz, Ayse Semra; Yis, Uluç; Ünalp, Aycan; Dündar, Nihal Olgaç; Ülgenalp, Ayfer; Erçal, Derya.
Afiliação
  • Gursoy S; Department of Pediatric Genetics, Dr. Behcet Uz Children's Hospital, Izmir, Turkey.
  • Ataman E; Department of Medical Genetics, Dokuz Eylül University Medical School, Izmir, Turkey.
  • Baysal BT; Department of Pediatric Neurology, Dr. Behcet Uz Children's Hospital, Izmir, Turkey.
  • Özyilmaz B; Department of Medical Genetics, Tepecik Training and Research Hospital, Izmir, Turkey.
  • Gençpinar P; Department of Pediatric Neurology, Tepecik Training and Research Hospital, Izmir, Turkey.
  • Hiz AS; Department of Pediatric Neurology, Dokuz Eylül University Medical School, Izmir, Turkey.
  • Yis U; Department of Pediatric Neurology, Dokuz Eylül University Medical School, Izmir, Turkey.
  • Ünalp A; Department of Pediatric Neurology, Dr. Behcet Uz Children's Hospital, Izmir, Turkey.
  • Dündar NO; Department of Pediatric Neurology, Tepecik Training and Research Hospital, Izmir, Turkey.
  • Ülgenalp A; Department of Medical Genetics, Dokuz Eylül University Medical School, Izmir, Turkey.
  • Erçal D; Department of Pediatric Genetics, Dokuz Eylül University Medical School, Izmir, Turkey.
Ann Indian Acad Neurol ; 23(2): 206-210, 2020.
Article em En | MEDLINE | ID: mdl-32189863
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Ann Indian Acad Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Turquia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Ann Indian Acad Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Turquia