Back to Search
Start Over
Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients.
- Source :
-
European journal of human genetics : EJHG [Eur J Hum Genet] 2020 Jan; Vol. 28 (1), pp. 138. - Publication Year :
- 2020
-
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.
Details
- Language :
- English
- ISSN :
- 1476-5438
- Volume :
- 28
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- European journal of human genetics : EJHG
- Accession number :
- 31477843
- Full Text :
- https://doi.org/10.1038/s41431-019-0394-5