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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2019 Apr 12;28(1):138. doi: 10.1038/s41431-019-0394-5

Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients

Roser Urreizti 1,✉,#, Klaus Mayer 2,#, Gilad D Evrony 3,#, Edith Said 4,5, Laura Castilla-Vallmanya 1, Neal A L Cody 6,7, Guillem Plasencia 8, Bruce D Gelb 6,9,10, Daniel Grinberg 1, Ulrich Brinkmann 2,#, Bryn D Webb 6,9,10,#, Susanna Balcells 1,#
PMCID: PMC6906502  PMID: 31477843

Correction to: Eur J Human Genet;

10.1038/s41431-019-0374-9;

published online 15 March 2019

Following the publication of the article, it was noted that the last column in Table 1, the total % should have read 5/8 (62.5) for the ‘Epilepsy’ row, and not 5.7 (71.4). This has now been amended in the HTML and PDF of the original article.


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

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