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Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder.
Khan, Hamid; Harripaul, Ricardo; Mikhailov, Anna; Herzi, Sumayah; Bowers, Sonya; Ayub, Muhammad; Shabbir, Muhammad Imran; Vincent, John B.
Afiliação
  • Khan H; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Centre for Addiction and Mental Health, 250 College St, Toronto, ON, M5T 1R8, Canada.
  • Harripaul R; Department of Biological Sciences, International Islamic University Islamabad, Islamabad, Pakistan.
  • Mikhailov A; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Centre for Addiction and Mental Health, 250 College St, Toronto, ON, M5T 1R8, Canada.
  • Herzi S; Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
  • Bowers S; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Centre for Addiction and Mental Health, 250 College St, Toronto, ON, M5T 1R8, Canada.
  • Ayub M; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Centre for Addiction and Mental Health, 250 College St, Toronto, ON, M5T 1R8, Canada.
  • Shabbir MI; Molecular Neuropsychiatry and Development (MiND) Lab, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Centre for Addiction and Mental Health, 250 College St, Toronto, ON, M5T 1R8, Canada.
  • Vincent JB; Department of Psychiatry, UCL, London, UK.
Sci Rep ; 14(1): 9230, 2024 04 22.
Article em En | MEDLINE | ID: mdl-38649688
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Transtorno do Espectro Autista / Sequenciamento do Exoma Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Transtorno do Espectro Autista / Sequenciamento do Exoma Limite: Child / Child, preschool / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Sci Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá