Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients (European Journal of Human Genetics, (2020), 28, 1, (64-75), 10.1038/s41431-019-0374-9)

Roser Urreizti, Klaus Mayer, Gilad D. Evrony, Edith Said, Laura Castilla-Vallmanya, Neal A.L. Cody, Guillem Plasencia, Bruce D. Gelb, Daniel Grinberg, Ulrich Brinkmann, Bryn D. Webb, Susanna Balcells

Research output: Contribution to journalComment/debate

2 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)138
Number of pages1
JournalEuropean Journal of Human Genetics
Volume28
Issue number1
DOIs
StatePublished - 1 Jan 2020

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