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Article

Clinical manifestations and BTK gene defect in 4 unrelated Taiwanese families with Bruton's disease.

Asian Pacific journal of allergy and immunology - 1 Sept 2011

Lee Kuo-Hsi, Shyur Shyh-Dar, Chu Szu-Hung, Huang Li-Hsin, Kao Yu-Hsuan, Lei Wei-Te, Cheng Chieh-Han, Lo Chia-Yi, Chen Chen-Kuan, Liu Ling-Chun

Abstract excerpt

BACKGROUND AND OBJECTIVE: X-linked agammaglobulinemia (XLA, also called Bruton's disease) is is an X-linked recessive disorder characterized by recurrent bacterial infections, usually occurring in the first few years of life. Here, we report the results of a BTK gene mutation screening study that was performed in Taiwanese families with the BTK gene defect to further understand the inheritance patterns of XLA...

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Source

Identifiers

PMID: 22053596

Genes

BTK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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