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Frequency of CNKSR2 mutation in the X-linked epilepsy-aphasia spectrum.
Damiano, John A; Burgess, Rosemary; Kivity, Sara; Lerman-Sagie, Tally; Afawi, Zaid; Scheffer, Ingrid E; Berkovic, Samuel F; Hildebrand, Michael S.
Affiliation
  • Damiano JA; Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
  • Burgess R; Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
  • Kivity S; Department of Pediatric Neurology and Epilepsy Center, Schneider Children's Medical Center of Israel, Petah Tiqva, Israel.
  • Lerman-Sagie T; Pediatric Neurology Unit, Epilepsy Clinic, Wolfson Medical Center, Holon, Israel.
  • Afawi Z; Pediatric Neurology Unit, Epilepsy Clinic, Wolfson Medical Center, Holon, Israel.
  • Scheffer IE; Sackler School of Medicine, Tel-Aviv University, Ramat Aviv, Israel.
  • Berkovic SF; Department of Medicine, Epilepsy Research Centre, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.
  • Hildebrand MS; Department of Paediatrics, Royal Children's Hospital, University of Melbourne, Parkville, Victoria, Australia.
Epilepsia ; 58(3): e40-e43, 2017 03.
Article in En | MEDLINE | ID: mdl-28098945
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aphasia / Spasms, Infantile / Adaptor Proteins, Signal Transducing / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Epilepsia Year: 2017 Document type: Article
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aphasia / Spasms, Infantile / Adaptor Proteins, Signal Transducing / Mutation Type of study: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male Language: En Journal: Epilepsia Year: 2017 Document type: Article