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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.
Afiliación
  • 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 en En | MEDLINE | ID: mdl-32887940
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos