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Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?
Berry, Gerard T; Freeze, Hudson H; Morava, Eva.
Afiliación
  • Berry GT; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Freeze HH; Human Genetics Program, Sanford Children's Health Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA.
  • Morava E; Department of Clinical Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
Epilepsia ; 62(2): 335-336, 2021 02.
Article en En | MEDLINE | ID: mdl-33576051
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Espasmos Infantiles Idioma: En Revista: Epilepsia Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
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PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Espasmos Infantiles Idioma: En Revista: Epilepsia Año: 2021 Tipo del documento: Article