Mutations in SCN3A cause early infantile epileptic encephalopathy-Reference-Cited by-同舟云学术

Mutations in SCN3A cause early infantile epileptic encephalopathy

Published:2018-03-30 Issue:4 Volume:83 Page:703-717
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Zaman Tariq¹,Helbig Ingo¹²³,Božović Ivana Babić⁴,DeBrosse Suzanne D.⁵,Bergqvist A. Christina¹,Wallis Kimberly⁵,Medne Livija⁶,Maver Aleš⁷,Peterlin Borut⁷,Helbig Katherine L.¹⁸^ORCID,Zhang Xiaohong¹,Goldberg Ethan M.¹³⁹^ORCID

Affiliation:

1. Division of Neurology, Department of Pediatrics; Children's Hospital of Philadelphia; Philadelphia PA

2. Department of Neuropediatrics; University Medical Center Schleswig-Holstein, Christian Albrecht University; Kiel Germany

3. Department of Neurology, Perelman School of Medicine; University of Pennsylvania; Philadelphia PA

4. Department of Biology and Medical Genetics, School of Medicine; University of Rijeka; Rijeka Croatia

5. Departments of Genetics and Genome Sciences, Pediatrics, and Neurology, and Center for Human Genetics; Case Western Reserve University School of Medicine; Cleveland OH

6. Division of Human Genetics, Department of Pediatrics, Individualized Medical Genetics Center; Children's Hospital of Philadelphia; Philadelphia PA

7. Clinical Institute of Medical Genetics; University Medical Centre Ljubljana; Ljubljana Slovenia

8. Division of Clinical Genomics; Ambry Genetics; Aliso Viejo CA

9. Department of Neuroscience, Perelman School of Medicine; University of Pennsylvania; Philadelphia PA

Funder

NIH

Burroughs Wellcome Fund Career Award for Medical Scientists

Burroughs Wellcome Fund

Career Award for Medical Scientists

Publisher

Wiley

Subject