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Article

Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease.

Genes - 27 Nov 2020

Escalera-Balsera Alba, Roman-Naranjo Pablo, Lopez-Escamez Jose Antonio

Abstract excerpt

Familial Meniere Disease (FMD) is a rare inner ear disorder characterized by episodic vertigo associated with sensorineural hearing loss, tinnitus and/or aural fullness. We conducted a systematic review to find sequencing studies segregating rare variants in FMD to obtain evidence to support candidate genes for MD. After evaluating the quality of the retrieved records, eight studies were selected to carry out a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 33260921
DOI: 10.3390/genes11121414
PMCID: PMC7761472

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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