Article info

Download PDFPDF
Original research
Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay

Authors

  1. Correspondence to Dr Stuart E Turvey, The University of British Columbia, Vancouver, British Columbia V5Z 4H4, Canada; sturvey{at}bcchr.ca; Dr Anna Lehman; anna.lehman{at}vch.ca
View Full Text

Citation

Mohajeri A, Vaseghi-Shanjani M, Rosenfeld JA, et al
Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay

Publication history

  • Received December 27, 2022
  • Accepted May 29, 2023
  • First published June 14, 2023.
Online issue publication 
October 24, 2023

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.