Back to Search Start Over

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

Authors :
Urreizti R
Mayer K
Evrony GD
Said E
Castilla-Vallmanya L
Cody NAL
Plasencia G
Gelb BD
Grinberg D
Brinkmann U
Webb BD
Balcells S
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