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)
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Article de revue
Este ítem está publicado en
European Journal of Human Genetics. 2021-07-15, vol. 29, n° 9, p. 1470-1471
Resumen en inglés
In the original publication of the article, consortium author lists were missing in the article. The details are as below.