Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss
更正:NCOA3 被确定为解释常染色体显性遗传进行性听力损失的新候选基因
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddab325
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