Article info

Download PDFPDF
Original article
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome

Authors

  1. Correspondence to Dr Marwan Shinawi, Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, One Children's Place, Northwest Tower, 9132, Campus Box 8116, St Louis, MO 63110, USA; Shinawi_M{at}kids.wustl.edu
View Full Text

Citation

DeSanto C, D'Aco K, Araujo GC, et al
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome

Publication history

  • Received February 16, 2015
  • Revised June 17, 2015
  • Accepted July 14, 2015
  • First published August 11, 2015.
Online issue publication 
December 09, 2016

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.