Your browser doesn't support javascript.
loading
Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.
Fernandez, Thomas V; Williams, Zsanett P; Kline, Tina; Rajendran, Shreenath; Augustine, Farhan; Wright, Nicole; Sullivan, Catherine A W; Olfson, Emily; Abdallah, Sarah B; Liu, Wenzhong; Hoffman, Ellen J; Gupta, Abha R; Singer, Harvey S.
Afiliação
  • Fernandez TV; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
  • Williams ZP; Department of Psychiatry, Yale University School of Medicine, New Haven, CT, United States America.
  • Kline T; Department of Psychiatry, Vanderbilt University School of Nursing, Nashville, TN, United States America.
  • Rajendran S; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.
  • Augustine F; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.
  • Wright N; Departments of Neurology and Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, United States America.
  • Sullivan CAW; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
  • Olfson E; Department of Pediatrics, Yale University School of Medicine, New Haven, CT, United States America.
  • Abdallah SB; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
  • Liu W; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
  • Hoffman EJ; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
  • Gupta AR; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
  • Singer HS; Yale Child Study Center, Yale University School of Medicine, New Haven, CT, United States America.
PLoS One ; 18(10): e0291978, 2023.
Article em En | MEDLINE | ID: mdl-37788244
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Tourette / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Tourette / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2023 Tipo de documento: Article