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Article

Identification of an SH2D1A mutation in a hypogammaglobulinemic male patient with a diagnosis of common variable immunodeficiency.

International journal of hematology - 1 Jul 2003

Aghamohammadi Asghar, Kanegane Hirokazu, Moein Mostafa, Farhoudi Abolhasan, Pourpak Zahra, Movahedi Masoud, Gharagozlou Mohammad, Zargar Ali Akabar Amir, Miyawaki Toshio

Abstract excerpt

Common variable immunodeficiency (CVID) is a highly heterogeneous disease with an unpredictable pattern. CVID appears to have an immunologic and clinical phenotype similar to some hereditary humoral immunodeficiencies, including X-linked lymphoproliferative disease (XLP). The differential diagnosis of CVID and XLP is clinically of importance, because the two diseases have markedly different prognoses and...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 12894850
DOI: 10.1007/BF02983239

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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