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)
TRIMOUILLE, Aurelien
Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
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Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
Language
EN
Article de revue
This item was published in
European Journal of Human Genetics. 2021-07-15, vol. 29, n° 9, p. 1470-1471
English Abstract
In the original publication of the article, consortium author lists were missing in the article. The details are as below.
In the original publication of the article, consortium author lists were missing in the article. The details are as below.Read less <