| Title: |
Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3) |
| Authors: |
Cuvertino, S; Hartill, V; Colyer, A; Garner, T; Nair, N; Al-Gazali, L; Canham, N; Faundes, V; Flinter, F; Hertecant, J; Holder-Espinasse, M; Jackson, B; Lynch, SA; Nadat, F; Narasimhan, VM; Peckham, M; Sellers, R; Seri, M; Montanari, F; Southgate, L; Squeo, GM; Trembath, R; van Heel, D; Venuto, S; Weisberg, D; Stals, K; Ellard, S; Barton, A; Kimber, SJ; Sheridan, E; Merla, G; Stevens, A; Johnson, CA; Banka, S |
| Source: |
Genetics in Medicine |
| Publisher Information: |
Springer Nature |
| Publication Year: |
2020 |
| Collection: |
Universidad de Chile: Repositorio académico |
| Document Type: |
article in journal/newspaper |
| File Description: |
application/pdf |
| Language: |
English |
| ISSN: |
15300366; 10983600 |
| Relation: |
https://repositorio.uchile.cl/handle/2250/190859 |
| DOI: |
10.1038/s41436-020-0784-7 |
| Availability: |
https://doi.org/10.1038/s41436-020-0784-7; https://repositorio.uchile.cl/handle/2250/190859 |
| Rights: |
Attribution-NonCommercial-NoDerivs 3.0 Chile ; http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ |
| Accession Number: |
edsbas.3F218EC8 |
| Database: |
BASE |