Skip to main content
PMC home page
European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2020 Feb 18;28(5):692. doi: 10.1038/s41431-020-0587-y

Correction: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

Soara Menabò 1,#, Seher Polat 2,#, Lilia Baldazzi 1, Alexandra E Kulle 3, Paul-Martin Holterhus 3, Joachim Grötzinger 4, Flaminia Fanelli 5, Antonio Balsamo 1,✉, Felix G Riepe 3
PMCID: PMC7171131  PMID: 32071409

Correction to: European Journal of Human Genetics

10.1038/ejhg.2013.197

In the originally published article, there are two cases where the pathogenic variant p.(Arg332Gln) was written as p.(Arg332Trp). The two cases of p.(Arg332Trp) should therefore be p.(Arg332Gln) in the original manuscript.

Footnotes

The original article can be found online at 10.1038/ejhg.2013.197.

These authors contributed equally: Soara Menabò, Seher Polat

These authors jointly supervised this work: Antonio Balsamo, Felix G. Riepe

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

RESOURCES