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Article

Unusual phenotype of heterozygous LOF mutation in IKZF1, with common variable immunodeficiency presenting initially as immune thrombocytopenia: A case report.

Journal of paediatrics and child health - 1 Dec 2022

Alzahrani Talal S, Al-Jabri Hassan, Elhomoudi Ayman

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Share to Common Variable Immunodeficiency
Share to Heterozygote
Share to Ikaros Transcription Factor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Purpura, Thrombocytopenic, Idiopathic

Share to Thrombocytopenia

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Identifiers

PMID: 35979904
DOI: 10.1111/jpc.16162

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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