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Article

Novel Mutation in SH2 Domain of STAT3 (p.M660T) in Hyper-IgE Syndrome with Sterno-Clavicular and Paravertebral Abscesses.

Indian journal of pediatrics - 1 Jun 2017

Saikia Biman, Goel Shubham, Suri Deepti, Minz Ranjana W, Rawat Amit, Singh Surjit

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 28315006
DOI: 10.1007/s12098-017-2336-y

Genes

STAT3

Variants

Provenance

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

Related research

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Novel Mutation in SH2 Domain of STAT3 (p.M660T) in Hyper-IgE Syndrome with Sterno-Clavicular and Paravertebral Abscesses.PMID 28315006Read ↗

Identification of a novel STAT3 mutation in a patient with hyper-IgE syndrome.Semantic proximity Read ↗

Hyper-IgE syndrome with a novel mutation of the STAT3 gene.Semantic proximity Read ↗

A novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene, in hyper-IgE syndrome.Semantic proximity Read ↗

Hyper-IgE syndrome with a novel STAT3 mutation-a single center study from India.Semantic proximity Read ↗

Disseminated BCG Disease in a Patient with Hyper IgE Syndrome due to Dominant-Negative STAT3 Mutation-Case Report.Semantic proximity Read ↗

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.Semantic proximity Read ↗

A novel STAT3 mutation in a patient with hyper-immunoglobulin E syndrome.Semantic proximity Read ↗

Hyper IgE syndrome: anaphylaxis in a patient carrying the N567D STAT3 mutation.Semantic proximity Read ↗

Autosomal dominant hyper IgE syndrome from a single centre in Chongqing, China (2009-2018).Semantic proximity Read ↗

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome.Semantic proximity Read ↗

Functional characterization of two new STAT3 mutations associated with hyper-IgE syndrome in a Mexican cohort.Semantic proximity Read ↗

Clinical Profile of Hyper-IgE Syndrome in India.Semantic proximity Read ↗

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