CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development-Reference-Cited by-同舟云学术

CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development

Published:2019-07-16 Issue:8 Volume:60 Page:1733-1742
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Demarest Scott T.¹²³⁴⁵^ORCID,Olson Heather E.⁶,Moss Angela²,Pestana‐Knight Elia⁷⁸⁹,Zhang Xiaoming⁷⁸⁹,Parikh Sumit⁹¹⁰,Swanson Lindsay C.⁶,Riley Katherine D.⁶,Bazin Grace A.⁶,Angione Katie¹³,Niestroj Lisa‐Marie¹¹^ORCID,Lal Dennis⁷⁹¹¹¹²¹³,Juarez‐Colunga Elizabeth²¹⁴,Benke Tim A.¹³⁴⁵¹⁵

Affiliation:

1. Children's Hospital Colorado Aurora Colorado

2. Adult and Child Consortium for Health Outcomes Research and Delivery Science Aurora Colorado

3. University of Colorado School of Medicine Aurora Colorado

4. Department of Pediatrics Colorado School of Public Health Aurora Colorado

5. Department of Neurology Colorado School of Public Health Aurora Colorado

6. Division of Epilepsy and Clinical Neurophysiology Department of Neurology Boston Children's Hospital Boston Massachusetts

7. Epilepsy Center, Neurological Institute Cleveland Clinic Cleveland Ohio

8. Department of Neurology Lerner Research Institute Cleveland Ohio

9. Genomic Medicine Institute Lerner Research Institute Cleveland Ohio

10. Department of Neurogenetics Lerner Research Institute Cleveland Ohio

11. Cologne Center for Genomics University of Cologne Cologne Germany