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NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.
Salazar-Silva R, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague E, Mingroni-Netto RC. Salazar-Silva R, et al. Among authors: nicastro fs. Hum Mol Genet. 2021 Jan 21;29(22):3691-3705. doi: 10.1093/hmg/ddaa240. Hum Mol Genet. 2021. PMID: 33326993 Free PMC article.
Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.
Salazar-Silva R, Dantas VLG, Alves LU, Batissoco AC, Oiticica J, Lawrence EA, Kawafi A, Yang Y, Nicastro FS, Novaes BC, Hammond C, Kague E, Mingroni-Netto RC. Salazar-Silva R, et al. Among authors: nicastro fs. Hum Mol Genet. 2021 Dec 17;31(1):156. doi: 10.1093/hmg/ddab325. Hum Mol Genet. 2021. PMID: 34788418 Free PMC article. No abstract available.
Changes in click characteristics during ABR recording.
Fávero ML, Silva FL, Tabith Junior A, Nicastro FS, Gudmond MC, Spinelli M. Fávero ML, et al. Among authors: nicastro fs. Braz J Otorhinolaryngol. 2007 Jan-Feb;73(1):7-11. doi: 10.1016/s1808-8694(15)31115-0. Braz J Otorhinolaryngol. 2007. PMID: 17505592 Free PMC article.