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

Overview of attention for article published in Journal of Medical Genetics, June 2023

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In the top 25% of all research outputs scored by Altmetric
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RT @TurveyLab: New human immunodeficiency disorder. Just published in @JMG_BMJ !

RT @JMG_BMJ: Dominant -ve IKZF2 variants cause ICHAD syndrome 👇 https://t.co/qflox0ct9P I mmunodysregulation C raniofacial H earing imp…

RT @TurveyLab: New human immunodeficiency disorder. Just published in @JMG_BMJ !

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