1. Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Issue 1 (11th November 2021) Authors: 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 Journal: Human molecular genetics Issue: Volume 31:Issue 1(2022) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Exome Sequencing Identifies a Novel Nonsense Mutation of MYO6 as the Cause of Deafness in a Brazilian Family. (17th October 2017) Authors: Sampaio‐Silva, Juliana; Batissoco, Ana Carla; Jesus‐Santos, Rafaela; Abath‐Neto, Osório; Scarpelli, Luciano Cesar; Nishimura, Patricia Yoshie; Galindo, Layla Testa; Bento, Ricardo Ferreira; Oiticica, Jeanne; Lezirovitz, Karina Journal: Annals of human genetics Issue: Volume 82:Number 1(2018:Jan.) Page Start: 23 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. (17th December 2020) Authors: da Silva, Rodrigo Salazar; 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; Netto, Regina Célia Mingroni Journal: Human molecular genetics Issue: Volume 29:Number 22(2020) Page Start: 3691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. (17th December 2020) Authors: 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 Journal: Human molecular genetics Issue: Volume 29:Number 22(2020) Page Start: 3691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗