Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss

The genetic heterogeneity of sensorineural hearing loss (SNHL) is a major hurdle to the detection of disease-causing variants. We aimed to identify underlying causal genes associated with mid-frequency hearing loss (HL), which contributes to less than about 1% of SNHL cases, by whole exome sequencin...

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Detalles Bibliográficos
Autores principales: Pavlenkova, Zuzana, Varga, Lukas, Borecka, Silvia, Karhanek, Miloslav, Huckova, Miloslava, Skopkova, Martina, Profant, Milan, Gasperikova, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602250/
https://www.ncbi.nlm.nih.gov/pubmed/34795337
http://dx.doi.org/10.1038/s41598-021-01876-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602250/
https://www.ncbi.nlm.nih.gov/pubmed/34795337
http://dx.doi.org/10.1038/s41598-021-01876-1

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