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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2016 Sep 15;24(10):1515. doi: 10.1038/ejhg.2016.51

Genetic and biochemical study of dual hereditary jaundice: Dubin–Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2

Lenka Slachtova, Ondrej Seda, Jana Behunova, Martin Mistrik, Pavel Martasek
PMCID: PMC5027691  PMID: 27628566

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.


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