CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development.
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| Title: | CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development. |
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| Authors: | Demarest ST; Children's Hospital Colorado, Aurora, Colorado.; Adult and Child Consortium for Health Outcomes Research and Delivery Science, Aurora, Colorado.; University of Colorado School of Medicine, Aurora, Colorado.; Department of Pediatrics, Colorado School of Public Health, Aurora, Colorado.; Department of Neurology, Colorado School of Public Health, Aurora, Colorado., Olson HE; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts., Moss A; Adult and Child Consortium for Health Outcomes Research and Delivery Science, Aurora, Colorado., Pestana-Knight E; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio.; Department of Neurology, Lerner Research Institute, Cleveland, Ohio.; Genomic Medicine Institute, Lerner Research Institute, Cleveland, Ohio., Zhang X; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio.; Department of Neurology, Lerner Research Institute, Cleveland, Ohio.; Genomic Medicine Institute, Lerner Research Institute, Cleveland, Ohio., Parikh S; Genomic Medicine Institute, Lerner Research Institute, Cleveland, Ohio.; Department of Neurogenetics, Lerner Research Institute, Cleveland, Ohio., Swanson LC; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts., Riley KD; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts., Bazin GA; Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts., Angione K; Children's Hospital Colorado, Aurora, Colorado.; University of Colorado School of Medicine, Aurora, Colorado., Niestroj LM; Cologne Center for Genomics, University of Cologne, Cologne, Germany., Lal D; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, Ohio.; Genomic Medicine Institute, Lerner Research Institute, Cleveland, Ohio.; Cologne Center for Genomics, University of Cologne, Cologne, Germany.; Cleveland Clinic Children's, Cleveland, Ohio.; Stanley Center for Psychiatric Research, Cambridge, Massachusetts.; Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts., Juarez-Colunga E; Adult and Child Consortium for Health Outcomes Research and Delivery Science, Aurora, Colorado.; Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, Colorado., Benke TA; Children's Hospital Colorado, Aurora, Colorado.; University of Colorado School of Medicine, Aurora, Colorado.; Department of Pediatrics, Colorado School of Public Health, Aurora, Colorado.; Department of Neurology, Colorado School of Public Health, Aurora, Colorado.; Department of Pharmacology, Colorado School of Public Health, Aurora, Colorado.; Department of Otolaryngology, Colorado School of Public Health, Aurora, Colorado. |
| Source: | Epilepsia [Epilepsia] 2019 Aug; Vol. 60 (8), pp. 1733-1742. Date of Electronic Publication: 2019 Jul 16. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 1528-1167 |
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| DOI: | 10.1111/epi.16285 |
