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Article

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease.

The Laryngoscope - 1 Jan 2010

Lopez-Escamez Jose A, Saenz-Lopez Pablo, Acosta Lourdes, Moreno Antonia, Gazquez Irene, Perez-Garrigues Herminio, Lopez-Nevot Alicia, Lopez-Nevot Miguel A

Abstract excerpt

OBJECTIVES/HYPOTHESIS: Bilateral Meniere's disease (BMD) is a severe disease that usually results in bilateral severe or profound sensorineural hearing loss and chronic disequilibrium with loss of vestibular function. We examined single nucleotide polymorphisms (SNPs) in the PTPN22 and CTLA4 gene...

Read the complete abstract on PubMed

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Genetic

Share to Polymorphism, Single Nucleotide

Share to Protein Tyrosine Phosphatases

Source

Identifiers

PMID: 19780033
DOI: 10.1002/lary.20650

Genes

PTPN22
CTLA4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19780033-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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