Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss

Adult-onset progressive hearing loss is a common, complex disease with a strong genetic component. Although to date over 150 genes have been identified as contributing to human hearing loss, many more remain to be discovered, as does most of the underlying genetic diversity. Many different variants...

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Detalles Bibliográficos
Autores principales: Lewis, Morag A., Schulte, Jennifer, Matthews, Lois, Vaden, Kenneth I., Steves, Claire J., Williams, Frances M.K., Schulte, Bradley A., Dubno, Judy R., Steel, Karen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168485/
https://www.ncbi.nlm.nih.gov/pubmed/37163093
http://dx.doi.org/10.1101/2023.04.27.23289040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168485/
https://www.ncbi.nlm.nih.gov/pubmed/37163093
http://dx.doi.org/10.1101/2023.04.27.23289040

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