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Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual development.
Thuresson, A-C; Van Buggenhout, G; Sheth, F; Kamate, M; Andrieux, J; Clayton Smith, J; Soussi Zander, C.
Affiliation
  • Thuresson AC; Department of Immunology, Genetics and Pathology, Rudbeck and Science for Life laboratory, Uppsala University, Uppsala, Sweden.
  • Van Buggenhout G; Center for Human Genetics, University Hospitals Leuven, Leuven, Belgium.
  • Sheth F; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Kamate M; FRIGE's Institute of Human Genetics, Ahmedabad, India.
  • Andrieux J; Department of Pediatric Neurology and Child Development Centre, KLES Prabhakar Kore Hospital, Belgaum, India.
  • Clayton Smith J; Laboratoire de Génétique Médicale, Hopital Jeanne de Flandre, CHRU de Lille, Lille, France.
  • Soussi Zander C; Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre, St Mary's Hospital, Manchester, UK.
Clin Genet ; 91(1): 106-110, 2017 01.
Article in En | MEDLINE | ID: mdl-27153334

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Sodium Channels / Genetic Predisposition to Disease / Gene Duplication / NAV1.2 Voltage-Gated Sodium Channel / NAV1.3 Voltage-Gated Sodium Channel Type of study: Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male / Newborn Language: En Journal: Clin Genet Year: 2017 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Sodium Channels / Genetic Predisposition to Disease / Gene Duplication / NAV1.2 Voltage-Gated Sodium Channel / NAV1.3 Voltage-Gated Sodium Channel Type of study: Risk_factors_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male / Newborn Language: En Journal: Clin Genet Year: 2017 Document type: Article Affiliation country: Country of publication: