Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Issue 1 (11th November 2021)

Record Type:: Journal Article
Title:: Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss. Issue 1 (11th November 2021)
Main Title:: Corrigendum to: NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss
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
Abstract:
Is Part Of:: Human molecular genetics. Volume 31:Issue 1(2022)
Journal:: Human molecular genetics
Issue:: Volume 31:Issue 1(2022)
Issue Display:: Volume 31, Issue 1 (2022)
Year:: 2022
Volume:: 31
Issue:: 1
Issue Sort Value:: 2022-0031-0001-0000
Page Start:: 156
Page End:: 156
Publication Date:: 2021-11-11
Subjects:: Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8
Journal URLs:: http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗
DOI:: 10.1093/hmg/ddab325 ↗
Languages:: English
ISSNs:: 0964-6906
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store
Ingest File:: 20287.xml