Correction: A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation.

Ganesan, Shiva; Galer, Peter D; Helbig, Katherine L; McKeown, Sarah E; O'Brien, Margaret; Gonzalez, Alexander K; Felmeister, Alex S; Khankhanian, Pouya; Ellis, Colin A; Helbig, Ingo.

Afiliação

Ganesan S; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Galer PD; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Helbig KL; Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
McKeown SE; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
O'Brien M; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Gonzalez AK; Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Felmeister AS; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Khankhanian P; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Ellis CA; Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Helbig I; Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Genet Med ; 22(11): 1921-1922, 2020 Nov.

Article em En | MEDLINE | ID: mdl-32887940

ABSTRACT

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article