Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genetics, (2021), 10.1038/s41431-021-00900-2) de, Boer, E , CW Ockeloen , Rita Horvath , Enzo Cohen , I Cuesta , Daniel Danis , A-S Denomme-Pichon , Yannis Duffourd , Christian Gilissen , Mridul Johari , Steven Laurie , S Li , Leslie Matalonga , Isabelle Nelson , Sophia Peters , Ida Paramonov , S Prasanth , Peter N. Robinson , Karolis Sablauskas , Marco Savarese , Wouter Steyaert , Ana Töpf , van, der, Velde, Jk , Antonio Vitobello , RJ Rodenburg , Mjh Coenen , M Janssen , D Henssen , Siddharth Banka , Elisa Benetti , G Casari , Andrea Ciolfi , Jill Clayton-Smith , Bruno Dallapiccola , Laurence Faivre , Tobias B. Haack , A Hammarsjo , Marketa Havlovicova , Alexander Hoischen , A Hugon , Adam Jackson , Tjitske Kleefstra , A Lindstrand , E Lopez-Martin , Milan Macek , Nigro , A Nordgren , M Pettersson , Michele Pinelli , Simone Pizzi , M Posada , Francesca Clementina Radio , Alessandra Renieri , Caroline Rooryck , L Ryba , M Schwarz , Marco Tartaglia , Christel Thauvin , Annalaura Torella , Alain Verloes , Lisenka E.L.M. Vissers , K Vyshka , Birte Zurek , Aurélien Trimouille , Lelm Vissers European Journal of Human Genetics（2021）
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epilepsy, intellectual disability, whole exome
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