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]
< Réduire
Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
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Ce document a été publié dans
European Journal of Human Genetics. 2021-07-15, vol. 29, n° 9, p. 1470-1471
Résumé en anglais
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.< Réduire
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