Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual...
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)
About this item
Full title
Author / Creator
de Boer, Elke , Ockeloen, Charlotte W. , Matalonga, Leslie , Horvath, Rita , Cohen, Enzo , Nelson, Isabelle , Rodenburg, Richard J. , Coenen, Marieke J. H. , Janssen, Mirian , Henssen, Dylan , Gilissen, Christian , Steyaert, Wouter , Paramonov, Ida , Trimouille, Aurelien , Kleefstra, Tjitske , Verloes, Alain and Vissers, Lisenka E. L. M.
Publisher
Nature Publishing Group
Journal title
Language
English
Formats
Publication information
Publisher
Nature Publishing Group
Subjects
More information
Alternative Titles
Full title
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)
Authors, Artists and Contributors
Author / Creator
Ockeloen, Charlotte W.
Matalonga, Leslie
Horvath, Rita
Cohen, Enzo
Nelson, Isabelle
Rodenburg, Richard J.
Coenen, Marieke J. H.
Janssen, Mirian
Henssen, Dylan
Gilissen, Christian
Steyaert, Wouter
Paramonov, Ida
Trimouille, Aurelien
Kleefstra, Tjitske
Verloes, Alain
Vissers, Lisenka E. L. M.
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_hal_primary_oai_HAL_hal_03403537v1
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_hal_primary_oai_HAL_hal_03403537v1
Other Identifiers
ISSN
1018-4813
E-ISSN
1476-5438
DOI
10.1038/s41431-021-00937-3