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) - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue European Journal of Human Genetics Année : 2021

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)

Rita Horvath
Enzo Cohen
  • Fonction : Auteur
  • PersonId : 1116862

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No abstract available

Dates et versions

hal-03403537 , version 1 (26-10-2021)

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Citer

Elke de Boer, Charlotte W. Ockeloen, Leslie Matalonga, Rita Horvath, Enzo Cohen, et al.. 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). European Journal of Human Genetics, 2021, 29 (9), pp.1470-1471. ⟨10.1038/s41431-021-00937-3⟩. ⟨hal-03403537⟩
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