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N-methyl-d-aspartate (NMDA) receptor genetics: The power of paralog homology and protein dynamics in defining dominant genetic variants.
Charron, Jacob G; Hernandez, Angel; Bilinovich, Stephanie M; Vogt, Daniel L; Bedinger, Laura A; Seaver, Laurie H; Williams, Michael; Devries, Seth; Campbell, Daniel B; Bupp, Caleb P; Prokop, Jeremy W.
Afiliação
  • Charron JG; Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, Michigan, USA.
  • Hernandez A; Department of Biology, Calvin University, Grand Rapids, Michigan, USA.
  • Bilinovich SM; Pediatric Neurology, Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA.
  • Vogt DL; Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, Michigan, USA.
  • Bedinger LA; Center for Research in Autism, Intellectual, and other Neurodevelopmental Disabilities, Michigan State University, East Lansing, Michigan, USA.
  • Seaver LH; Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, Michigan, USA.
  • Williams M; Center for Research in Autism, Intellectual, and other Neurodevelopmental Disabilities, Michigan State University, East Lansing, Michigan, USA.
  • Devries S; Division of Medical Genetics, Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA.
  • Campbell DB; Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, Michigan, USA.
  • Bupp CP; Division of Medical Genetics, Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA.
  • Prokop JW; Department of Pediatrics and Human Development, Michigan State University, Grand Rapids, Michigan, USA.
Am J Med Genet A ; 188(2): 556-568, 2022 02.
Article em En | MEDLINE | ID: mdl-34726335
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Transtorno do Espectro Autista Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Transtorno do Espectro Autista Idioma: En Ano de publicação: 2022 Tipo de documento: Article