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Article

Autosomal recessive agammaglobulinemic patient with a novel large deletion in IGHM presenting with mild clinical phenotype.

Clinical immunology (Orlando, Fla.) - 1 Jan 2020

Nain Ercan, Ulgen Ozge, Kiykim Ayca, Aydiner Elif Karakoc, Ozen Ahmet, Baris Safa

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Share to Agammaglobulinemia
Share to Child, Preschool
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31683053
DOI: 10.1016/j.clim.2019.108295

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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