Associated Papers
An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population.
Parra-Perez AM et al.
Human Genetics, 2024
Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease.
Escalera-Balsera A et al.
Genes, 2020
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.
Roman-Naranjo P et al.
Ear and Hearing, 0
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