Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis
-
Published:2021-07-15
Issue:9
Volume:29
Page:1470-1471
-
ISSN:1018-4813
-
Container-title:European Journal of Human Genetics
-
language:en
-
Short-container-title:Eur J Hum Genet
Author:
de Boer Elke, Ockeloen Charlotte W.ORCID, Matalonga Leslie, Horvath RitaORCID, Cohen Enzo, Cuesta Isabel, Danis Daniel, Denommé-Pichon Anne-Sophie, Duffourd Yannis, Gilissen Christian, Johari Mridul, Laurie Steven, Li Shuang, Matalonga Leslie, Nelson Isabelle, Peters Sophia, Paramonov Ida, Prasanth Sivakumar, Robinson Peter, Sablauskas Karolis, Savarese Marco, Steyaert Wouter, Töpf Ana, van der Velde Joeri K., Vitobello Antonio, Rodenburg Richard J.ORCID, Coenen Marieke J. H., Janssen Mirian, Henssen Dylan, Gilissen ChristianORCID, Steyaert WouterORCID, Paramonov Ida, Banka Siddharth, Benetti Elisa, Casari Giorgio, Ciolfi Andrea, Clayton-Smith Jill, Dallapiccola Bruno, de Boer Elke, Faivre Laurence, Haack Tobias B., Hammarsjö Anna, Havlovicova Marketa, Hoischen Alexander, Hugon Anne, Jackson Adam, Kleefstra Tjitske, Lindstrand Anna, López-Martín Estrella, Macek Milan, Nigro Vicenzo, Nordgren Ann, Pettersson Maria, Pinelli Michele, Pizzi Simone, Posada Manuel, Radio Francesca Clementina, Renieri Alessandra, Rooryck Caroline, Ryba Lukas, Schwarz Martin, Tartaglia Marco, Thauvin Christel, Torella Annalaura, Verloes Alain, Vissers Lisenka, Vyshka Klea, Zurek Birte, Trimouille AurélienORCID, Kleefstra Tjitske, Verloes AlainORCID, Vissers Lisenka E. L. M.ORCID, ,
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
|
|