New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease

The objective was to study the genetic etiology of Ménière’s disease (MD) using next-generation sequencing in three families with three cases of MD. Whole exome sequencing was used to identify rare genetic variants co-segregating with MD in Finnish families. In silico estimations and population data...

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Detalles Bibliográficos
Autores principales: Skarp, Sini, Korvala, Johanna, Kotimäki, Jouko, Sorri, Martti, Männikkö, Minna, Hietikko, Elina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222295/
https://www.ncbi.nlm.nih.gov/pubmed/35741759
http://dx.doi.org/10.3390/genes13060998

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222295/
https://www.ncbi.nlm.nih.gov/pubmed/35741759
http://dx.doi.org/10.3390/genes13060998

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