Pathogenic Variants in TNRC6B Cause a Genetic Disorder Characterised by Developmental Delay/intellectual Disability and a Spectrum of Neurobehavioural Phenotypes Including Autism and ADHD Jorge Luis Granadillo , Alexander P.A. Stegmann , Hui Guo , Kun Xia , Brad Angle , Kelly Bontempo , Judith D. Ranells , Patricia Newkirk , Carrie Costin , Joleen Viront , Constanze T. Stumpel , Margje Sinnema , Bianca Panis , Rolph Pfundt , Ingrid P. C. Krapels , Merel Klaassens , Joost Nicolai , Jinliang Li , Yuwu Jiang , Elysa Marco , Ana Canton , Ana Claudia Latronico , Luciana Montenegro , Bruno Leheup , Celine Bonnet , Shivarajan M. Amudhavalli , Caitlin E. Lawson , Kirsty McWalter , Aida Telegrafi , Richard Pearson , Malin Kvarnung , Xia Wang , Weimin Bi , Jill Anne Rosenfeld , Marwan Shinawi Journal of Medical Genetics（2020）
Key words
ADHD, autism, autosomal dominant, De novo, developmental delay
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