Article info
PDFNovel disease loci
Original research
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
- Correspondence to Dr Marwan Shinawi, Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine in Saint Louis, St. Louis, MO 63110, USA; Mshinawi{at}wustl.edu
Citation
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD
Publication history
- Received September 12, 2019
- Revised January 23, 2020
- Accepted January 24, 2020
- First published March 9, 2020.
Online issue publication
September 22, 2020
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© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.