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

Original languageEnglish
Pages (from-to)1470-1471
Number of pages2
JournalEuropean Journal of Human Genetics
Issue number9
Publication statusPublished - Sept 2021


Dive into the research topics of '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)'. Together they form a unique fingerprint.

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