Correction to: European Journal of Human Genetics (2016) 24, 704–709; doi:10.1038/ejhg.2015.181; published online 9 September 2015
Post publication, the authors realised that they had omitted the following acknowledgement:
PM is also supported by Grant Agency of Czech Republic (14-36804G).
The authors would like to apologise for this omission.
Additional information
The online version of the original article can be found at 10.1038/ejhg.2015.181
Rights and permissions
About this article
Cite this article
Slachtova, L., Seda, O., Behunova, J. et al. Erratum: Genetic and biochemical study of dual hereditary jaundice: Dubin–Johnson and Gilbert’s syndromes. Haplotyping and founder effect of deletion in ABCC2. Eur J Hum Genet 24, 1515 (2016). https://doi.org/10.1038/ejhg.2016.51
Published:
Issue Date:
DOI: https://doi.org/10.1038/ejhg.2016.51
