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Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ3 Variant.
Arredondo, Kristen; Myers, Cortlandt; Hansen-Kiss, Emily; Mathew, Mariam T; Jayaraman, Vijayakumar; Siemon, Amy; Bartholomew, Dennis; Herman, Gail E; Mori, Mari.
  • Arredondo K; Department of Pediatrics, 12306The Ohio State University, Columbus, OH, USA.
  • Myers C; Division of Pediatric Neurology, 2650Nationwide Children's Hospital, Columbus, OH, USA.
  • Hansen-Kiss E; Division of Genetic & Genomic Medicine, 2650Nationwide Children's Hospital, Columbus, OH, USA.
  • Mathew MT; Department of Diagnostic & Biomedical Sciences, 12340University of Texas Health Science Center at Houston, School of Dentistry, Houston, TX, USA.
  • Jayaraman V; Department of Pediatrics, 12306The Ohio State University, Columbus, OH, USA.
  • Siemon A; Institute for Genomic Medicine, 2650Nationwide Children's Hospital, Columbus, OH, USA.
  • Bartholomew D; Institute for Genomic Medicine, 2650Nationwide Children's Hospital, Columbus, OH, USA.
  • Herman GE; Division of Genetic & Genomic Medicine, 2650Nationwide Children's Hospital, Columbus, OH, USA.
  • Mori M; Department of Pediatrics, 12306The Ohio State University, Columbus, OH, USA.
J Child Neurol ; 37(6): 517-523, 2022 05.
Article en En | MEDLINE | ID: mdl-35384780
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Epilepsia Benigna Neonatal / Epilepsia / Canal de Potasio KCNQ3 Tipo de estudio: Prognostic_studies Límite: Adult / Child / Humans / Newborn Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Epilepsia Benigna Neonatal / Epilepsia / Canal de Potasio KCNQ3 Tipo de estudio: Prognostic_studies Límite: Adult / Child / Humans / Newborn Idioma: En Año: 2022 Tipo del documento: Article