Back to Search
Start Over
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study (European Journal of Human Genetics, (2020), 28, 5, (587-596), 10.1038/s41431-019-0553-8).
- Publication Year :
- 2020
-
Abstract
- 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)".Copyright © 2020, The Author(s), under exclusive licence to European Society of Human Genetics.
Details
- Database :
- OAIster
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1305122396
- Document Type :
- Electronic Resource