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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2020 Nov 9;29(2):363. doi: 10.1038/s41431-020-00750-4

Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study

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,✉
PMCID: PMC7868367  PMID: 33168987

Correction to: European Journal of Human Genetics

10.1038/s41431-019-0553-8

In Table 3, on pages 591–592 of the original article, in the fourth row of the table, an alteration in GJB2 is shown as “c.429G>A p.(Glu147Lys)”, but it should read “c.439G>A p.(Glu147Lys)”.

Footnotes

The original article can be found online at 10.1038/s41431-019-0553-8.

Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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