Correction: Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy
Eur J Hum Genet
.
2021 May;29(5):887.
doi: 10.1038/s41431-021-00843-8.
Authors
Johann Kaspar Lieberwirth
1
,
Pascal Joset
2
,
Anja Heinze
1
,
Julia Hentschel
1
,
Anja Stein
3
,
Antonella Iannaccone
4
,
Katharina Steindl
2
,
Alma Kuechler
#
5
,
Rami Abou Jamra
#
6
Affiliations
1
Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany.
2
Institute of Medical Genetics, University of Zurich, Schlieren, Switzerland.
3
Department of Pediatrics I, Division of Neonatology, University Medical Center Essen, University Duisburg-Essen, Essen, Germany.
4
Department of Gynecology and Obstetrics, University Medical Center Essen, University Duisburg-Essen, Essen, Germany.
5
Institute of Human Genetics, University Medical Center Essen, University of Duisburg-Essen, Essen, Germany.
[email protected]
.
6
Institute of Human Genetics, University Medical Center Leipzig, Leipzig, Germany.
[email protected]
.
#
Contributed equally.
PMID:
33750920
PMCID:
PMC8110977
DOI:
10.1038/s41431-021-00843-8
No abstract available
Publication types
Published Erratum