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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis

Lookup NU author(s): Dr Ana TopfORCiD

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Abstract

© The Author(s), under exclusive licence to European Society of Human Genetics 2021In the original publication of the article, consortium author lists were missing in the article. The details are as below.

Publication metadata

Author(s): de Boer E, Ockeloen CW, Horvath R, Cohen E, Cuesta I, Danis D, Denomme-Pichon A-S, Duffourd Y, Gilissen C, Johari M, Laurie S, Li S, Matalonga L, Matalonga L, Nelson I, Peters S, Paramonov I, Prasanth S, Robinson P, Sablauskas K, Savarese M, Steyaert W, Steyaert W, Topf A, van der Velde JK, Vitobello A, Rodenburg RJ, Coenen MJH, Janssen M, Henssen D, Gilissen C, Paramonov I, Banka S, Benetti E, Casari G, Ciolfi A, Clayton-Smith J, Dallapiccola B, de Boer E, Faivre L, Haack TB, Hammarsjo A, Havlovicova M, Hoischen A, Hugon A, Jackson A, Kleefstra T, Lindstrand A, Lopez-Martin E, Macek M, Nigro V, Nordgren A, Pettersson M, Pinelli M, Pizzi S, Posada M, Radio FC, Renieri A, Rooryck C, Ryba L, Schwarz M, Tartaglia M, Thauvin C, Torella A, Verloes A, Vissers L, Vyshka K, Zurek B, Trimouille A, Kleefstra T, Verloes A, Vissers LELM

Publication type: Note

Publication status: Published

Journal: European Journal of Human Genetics

Year: 2021

Volume: 29

Pages: 1470-1471

Print publication date: 01/09/2021

Online publication date: 15/07/2021

Acceptance date: 02/04/2020

ISSN (print): 1018-4813

ISSN (electronic): 1476-5438

Publisher: Springer Nature

URL: https://doi.org/10.1038/s41431-021-00937-3

DOI: 10.1038/s41431-021-00937-3

PubMed id: 34267341

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