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Paper Details

Genomic analysis of "microphenotypes" in epilepsy.
Am J Med Genet A
2
2022
Epilepsy, GRIN2A, Jeavons syndrome, Landau-Kleffner, MECP2, SCN1A, SCN2A, SCN8A, epilepsies, epilepsy, focal epilepsy, genetic generalized epilepsy, patients, pediatric status epilepticus
Author NameAffiliation
Marta Amengual-GualDivision of Epilepsy and Clinical Neurophysiology, Boston Children's Hospital
Justice ClarkBoston Children's Hospital
Dmitry TchapyjnikovDuke University
Orrin DevinskyNew York University
Gianpiero L CavalleriSchool of Pharmacy and Biomedical Sciences, and FutureNeuro Research Centre, Royal College of Surgeons in Ireland
Chantal DepondtErasmus Hospital
Arjune SenUniversity of Oxford Nuffield
Terence J O'BrienMonash University
Erin L HeinzenUniversity of North Carolina System
Tobias LoddenkemperBoston Children's Hospital
David B GoldsteinInstitute for Genomic Medicine, Columbia Presbyterian Medical Center
David B GoldsteinInstitute for Genomic Medicine, Columbia Presbyterian Medical Center
Mohamad A MikatiDuke University School of Medicine
Norman DelantyBeaumont Hospital, School of Pharmacy and Biomedical Sciences, and FutureNeuro Research Centre, Royal College of Surgeons in Ireland
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Release 1.2