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Article

Large BTK gene mutation in a child with X-linked agammaglobulinemia and polyarthritis.

Clinical immunology (Orlando, Fla.) - 1 Oct 2017

Sharma Dhrubajyoti, Gupta Aman, Goel Shubham, Sharma Madhubala, Rawat Amit, Singh Surjit

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Share to Agammaglobulinaemia Tyrosine Kinase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28807838
DOI: 10.1016/j.clim.2017.08.005

Genes

BTK

Provenance

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

Related research

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Large BTK gene mutation in a child with X-linked agammaglobulinemia and polyarthritis.PMID 28807838Read ↗

X-linked agammaglobulinemia in two siblings with a novel mutation in the BTK gene who presented with polyarticular juvenile idiopathic arthritis.Semantic proximity Read ↗

BTK gene mutation in two non-identical twins with X-linked agammaglobulinemia associated with polyarticular juvenile idiopathic arthritis.Semantic proximity Read ↗

The spectrum of mutations in Btk that cause X-linked agammaglobulinemia.Semantic proximity Read ↗

A deep intronic BTK variant underlies X-linked agammaglobulinemia.Semantic proximity Read ↗

X-linked agammaglobulinemia: lack of mature B lineage cells caused by mutations in the Btk kinase.Semantic proximity Read ↗

Identification of 22 novel BTK gene variants in B cell deficiency with hypogammaglobulinemia.Semantic proximity Read ↗

X-Linked Agammaglobulinemia A Clinical and Molecular AnalysisSemantic proximity Read ↗

A novel Bruton's tyrosine kinase gene (BTK) invariant splice site mutation in a Malaysian family with X-linked agammaglobulinemia.Semantic proximity Read ↗

Identification by whole-exome sequencing of novel mutation c.64C > G in the BTK gene of a fetus with X-linked agammaglobulinemia.Semantic proximity Read ↗

Bruton's tyrosine kinase mutations in 8 Chinese families with X-linked agammaglobulinemia.Semantic proximity Read ↗

Clinical and genetic profiles of patients with X-linked agammaglobulinemia from southeast Turkey: Novel mutations in BTK gene.Semantic proximity Read ↗

An exon-skipping mutation in the btk gene of a patient with X-linked agammaglobulinemia and isolated growth hormone deficiency.Semantic proximity Read ↗

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