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)

Solve-RD SNV-indel working group; Solve-RD DITF-ITHACA

doi:10.1038/s41431-021-00937-3

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)

Solve-RD SNV-indel working group, Solve-RD DITF-ITHACA

Research output: Contribution to journal › Commentary/debate › peer-review

Abstract

In the original publication of the article, consortium author lists were missing in the article. The details are as below.

Original language	English
Pages (from-to)	1470-1471
Number of pages	2
Journal	European Journal of Human Genetics
Volume	29
Issue number	9
DOIs	https://doi.org/10.1038/s41431-021-00937-3
Publication status	Published - Sept 2021

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Solve-RD SNV-indel working group, & Solve-RD DITF-ITHACA (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). European Journal of Human Genetics, 29(9), 1470-1471. https://doi.org/10.1038/s41431-021-00937-3

Solve-RD SNV-indel working group ; Solve-RD DITF-ITHACA. / 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). In: European Journal of Human Genetics. 2021 ; Vol. 29, No. 9. pp. 1470-1471.

@article{f18808ecee5348bba51277557f36e893,

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)",

abstract = "In the original publication of the article, consortium author lists were missing in the article. The details are as below.",

author = "{Solve-RD SNV-indel working group} and {Solve-RD DITF-ITHACA} and {de Boer}, Elke and Ockeloen, {Charlotte W.} and Leslie Matalonga and Rita Horvath and Enzo Cohen and Isabel Cuesta and Daniel Danis and Denomm{\'e}-Pichon, {Anne Sophie} and Yannis Duffourd and Christian Gilissen and Mridul Johari and Steven Laurie and Shuang Li and Leslie Matalonga and Isabelle Nelson and Sophia Peters and Ida Paramonov and Sivakumar Prasanth and Karolis Sablauskas and Marco Savarese and Wouter Steyaert and Ana T{\"o}pf and {van der Velde}, {Joeri K.} and Antonio Vitobello and Rodenburg, {Richard J.} and Coenen, {Marieke J.H.} and Mirian Janssen and Dylan Henssen and Christian Gilissen and Wouter Steyaert and Ida Paramonov and Siddharth Banka and Elisa Benetti and Giorgio Casari and Andrea Ciolfi and Jill Clayton-Smith and Bruno Dallapiccola and {de Boer}, Elke and Laurence Faivre and Haack, {Tobias B.} and Anna Hammarsj{\"o} and Marketa Havlovicova and Alexander Hoischen and Anne Hugon and Adam Jackson and Tjitske Kleefstra and Anna Lindstrand and Estrella L{\'o}pez-Mart{\'i}n and Milan Macek and Vicenzo Nigro",

note = "Publisher Copyright: {\textcopyright} The Author(s), under exclusive licence to European Society of Human Genetics 2021",

year = "2021",

month = sep,

doi = "10.1038/s41431-021-00937-3",

language = "English",

volume = "29",

pages = "1470--1471",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

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Solve-RD SNV-indel working group & Solve-RD DITF-ITHACA 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)', European Journal of Human Genetics, vol. 29, no. 9, pp. 1470-1471. https://doi.org/10.1038/s41431-021-00937-3

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). / Solve-RD SNV-indel working group; Solve-RD DITF-ITHACA.
In: European Journal of Human Genetics, Vol. 29, No. 9, 09.2021, p. 1470-1471.

Research output: Contribution to journal › Commentary/debate › peer-review

TY - JOUR

T1 - Correction

T2 - 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)

AU - Solve-RD SNV-indel working group

AU - Solve-RD DITF-ITHACA

AU - de Boer, Elke

AU - Ockeloen, Charlotte W.

AU - Matalonga, Leslie

AU - Horvath, Rita

AU - Cohen, Enzo

AU - Cuesta, Isabel

AU - Danis, Daniel

AU - Denommé-Pichon, Anne Sophie

AU - Duffourd, Yannis

AU - Gilissen, Christian

AU - Johari, Mridul

AU - Laurie, Steven

AU - Li, Shuang

AU - Matalonga, Leslie

AU - Nelson, Isabelle

AU - Peters, Sophia

AU - Paramonov, Ida

AU - Prasanth, Sivakumar

AU - Sablauskas, Karolis

AU - Savarese, Marco

AU - Steyaert, Wouter

AU - Töpf, Ana

AU - van der Velde, Joeri K.

AU - Vitobello, Antonio

AU - Rodenburg, Richard J.

AU - Coenen, Marieke J.H.

AU - Janssen, Mirian

AU - Henssen, Dylan

AU - Gilissen, Christian

AU - Steyaert, Wouter

AU - Paramonov, Ida

AU - Banka, Siddharth

AU - Benetti, Elisa

AU - Casari, Giorgio

AU - Ciolfi, Andrea

AU - Clayton-Smith, Jill

AU - Dallapiccola, Bruno

AU - de Boer, Elke

AU - Faivre, Laurence

AU - Haack, Tobias B.

AU - Hammarsjö, Anna

AU - Havlovicova, Marketa

AU - Hoischen, Alexander

AU - Hugon, Anne

AU - Jackson, Adam

AU - Kleefstra, Tjitske

AU - Lindstrand, Anna

AU - López-Martín, Estrella

AU - Macek, Milan

AU - Nigro, Vicenzo

PY - 2021/9

Y1 - 2021/9

N2 - In the original publication of the article, consortium author lists were missing in the article. The details are as below.

AB - In the original publication of the article, consortium author lists were missing in the article. The details are as below.

UR - http://www.scopus.com/inward/record.url?scp=85111992488&partnerID=8YFLogxK

U2 - 10.1038/s41431-021-00937-3

DO - 10.1038/s41431-021-00937-3

M3 - Commentary/debate

C2 - 34267341

AN - SCOPUS:85111992488

SN - 1018-4813

VL - 29

SP - 1470

EP - 1471

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -

Solve-RD SNV-indel working group, Solve-RD DITF-ITHACA. 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 Sept;29(9):1470-1471. doi: 10.1038/s41431-021-00937-3

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)

Abstract

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