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), 29, 9, (1359-1368), 10.1038/s41431-021-00900-2)

Solve-RD SNV-indel working group, Solve-RD-DITF-ITHACA, Elke de Boer, Charlotte W. Ockeloen*, Leslie Matalonga, Rita Horvath, Richard J. Rodenburg, Marieke J.H. Coenen, Mirian Janssen, Dylan Henssen, Christian Gilissen, Wouter Steyaert, Ida Paramonov, Aurélien Trimouille, Tjitske Kleefstra, Alain Verloes, Lisenka E. L. M. Vissers

*Bijbehorende auteur voor dit werk

    OnderzoeksoutputAcademic

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    In the original publication of the article, consortium author lists were missing in the article. The details are as below.

    Originele taal-2English
    Pagina's (van-tot)1470-1471
    Aantal pagina's2
    TijdschriftEuropean Journal of Human Genetics
    Volume29
    Nummer van het tijdschrift9
    DOI's
    StatusPublished - sep-2021

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