NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

Hearing loss is a frequent sensory impairment in humans and genetic factors account for an elevated fraction of the cases. We have investigated a large family of five generations, with 15 reported individuals presenting non-syndromic, sensorineural, bilateral and progressive hearing loss, segregatin...

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Опубликовано в: :Hum Mol Genet
Главные авторы: Salazar-Silva, R, Dantas, Vitor Lima Goes, Alves, Leandro Ucela, Batissoco, Ana Carla, Oiticica, Jeanne, Lawrence, Elizabeth A, Kawafi, Abdelwahab, Yang, Yushi, Nicastro, Fernanda Stávale, Novaes, Beatriz Caiuby, Hammond, Chrissy, Kague, Erika, Mingroni-Netto, R C
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2020
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General Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7823111/
https://ncbi.nlm.nih.gov/pubmed/33326993
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddaa240
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