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Delineating the epilepsy phenotype of NGLY1 deficiency.
Levy, Rebecca J; Frater, Christina H; Gallentine, William B; Phillips, Jennifer M; Ruzhnikov, Maura R.
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  • Levy RJ; Department of Child Neurology, Lucile Packard Children's Hospital, Stanford University, Stanford, California, USA.
  • Frater CH; Department of Medical Genetics, Lucile Packard Children's Hospital, Stanford University, Stanford, California, USA.
  • Gallentine WB; Department of Child Neurology, Lucile Packard Children's Hospital, Stanford University, Stanford, California, USA.
  • Phillips JM; Department of Child Neurology, Lucile Packard Children's Hospital, Stanford University, Stanford, California, USA.
  • Ruzhnikov MR; Department of Child and Adolescent Psychiatry, Lucile Packard Children's Hospital, Stanford University, Stanford, California, USA.
J Inherit Metab Dis ; 45(3): 571-583, 2022 05.
Article en En | MEDLINE | ID: mdl-35243670
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epilepsia Tipo de estudio: Observational_studies Límite: Child, preschool / Humans Idioma: En Revista: J Inherit Metab Dis Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epilepsia Tipo de estudio: Observational_studies Límite: Child, preschool / Humans Idioma: En Revista: J Inherit Metab Dis Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos