Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay
Article in Journal of Medical Genetics (June 2023)
The most recent citing publications are shown below. View all 16 publications that cite this research output on Dimensions.
Article in Journal of Medical Genetics (June 2023)
Article in Postępy Biologii Komórki (March 2017)
Article in Scandinavian Journal of Immunology (March 2016)