Novel gene discovery for hearing loss and other routes to increased diagnostic rates

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Abstract

Despite decades of research, there is much to be learned about the genetic landscape of sensorineural hearing loss. Novel genes for hearing loss remain to be identified while ‘secrets’ of the known genes need to be uncovered. These ‘secrets’ include regulatory mechanisms of gene activity and novel aspects of gene structure. To obtain a more complete picture of the genetics of hearing loss, the available experimental and bioinformatic tools need to be fully exploited. This is also true for data resources such as ENCODE. For the inner ear, however, such data resources and analytical tools need to be developed or extended. Collaborative studies provide opportunities to achieve this and to optimally use those tools and resources that are already available. This will accelerate the discoveries that are necessary for improving molecular genetic diagnostics and genetic counselling and for the development of therapeutic strategies.

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APA

Kremer, H. (2022). Novel gene discovery for hearing loss and other routes to increased diagnostic rates. Human Genetics, 141(3–4), 383–386. https://doi.org/10.1007/s00439-021-02374-0

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