Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Eur J Hum Genet
.
2021 Feb;29(2):363.
doi: 10.1038/s41431-020-00750-4.
Authors
Lilian Downie
1
2
3
4
,
Jane Halliday
2
4
,
Rachel Burt
2
4
,
Sebastian Lunke
1
2
4
,
Elly Lynch
1
2
5
,
Melissa Martyn
2
4
5
,
Zeffie Poulakis
2
3
4
,
Clara Gaff
4
5
,
Valerie Sung
2
3
4
,
Melissa Wake
2
4
,
Matthew F Hunter
6
7
,
Kerryn Saunders
6
7
,
Elizabeth Rose
2
3
4
,
Sharon Lewis
2
4
,
Anna Jarmolowicz
1
2
,
Dean Phelan
1
2
,
Heidi L Rehm
8
;
Melbourne Genomics Health Alliance
;
David J Amor
9
10
11
12
Affiliations
1
Victorian Clinical Genetics Services, Melbourne, VIC, Australia.
2
Murdoch Children's Research Institute, Melbourne, VIC, Australia.
3
Royal Children's Hospital, Melbourne, VIC, Australia.
4
Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.
5
Melbourne Genomics Health Alliance, Melbourne, VIC, Australia.
6
Monash Health, Melbourne, VIC, Australia.
7
Monash University, Melbourne, VIC, Australia.
8
Massachusetts General Hospital and the Broad Institute of MIT and Harvard, Boston, MA, USA.
9
Victorian Clinical Genetics Services, Melbourne, VIC, Australia. david.amor@mcri.edu.au.
10
Murdoch Children's Research Institute, Melbourne, VIC, Australia. david.amor@mcri.edu.au.
11
Royal Children's Hospital, Melbourne, VIC, Australia. david.amor@mcri.edu.au.
12
Department of Paediatrics, University of Melbourne, Melbourne, VIC, Australia. david.amor@mcri.edu.au.
PMID:
33168987
PMCID:
PMC7868367
DOI:
10.1038/s41431-020-00750-4
No abstract available
Publication types
Published Erratum