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Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization.
Sheikh, Taimoor I; Harripaul, Ricardo; Vasli, Nasim; Ghadami, Majid; Santangelo, Susan L; Ayub, Muhammad; Sasanfar, Roksana; Vincent, John B.
  • Sheikh TI; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON M5T 1R8, Canada.
  • Harripaul R; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON M5T 1R8, Canada.
  • Vasli N; Institute of Medical Science, University of Toronto, Toronto, ON M5S 1A8, Canada.
  • Ghadami M; Department of Pediatric Laboratory Medicine, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
  • Santangelo SL; Department of Educational Sciences, Farhangian University, Tehran 19989-63341, Iran.
  • Ayub M; Center for Psychiatric Research, Maine Medical Center Research Institute, Portland, ME 04101, USA.
  • Sasanfar R; Department of Psychiatry, Tufts University School of Medicine, Boston, MA 02110, USA.
  • Vincent JB; Department of Psychiatry, Maine Medical Center, Portland, ME 04102, USA.
Genes (Basel) ; 13(1)2021 12 24.
Article en En | MEDLINE | ID: mdl-35052391
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Nucléolo Celular / Proteínas de Unión al ARN / Trastorno del Espectro Autista / Heterocigoto / Mutación Límite: Humans / Male Idioma: En Año: 2021 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfoproteínas / Nucléolo Celular / Proteínas de Unión al ARN / Trastorno del Espectro Autista / Heterocigoto / Mutación Límite: Humans / Male Idioma: En Año: 2021 Tipo del documento: Article