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  3. Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.

Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.

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DOI
10.48350/195568
Publisher DOI
10.1038/s41431-024-01606-x
PubMed ID
38565641
Date Issued
2024-09
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
en
Author(s)
Paulet, Alix
Bennett-Ness, Cavan
Ageorges, Faustine
Trost, Detlef
Green, Andrew
Goudie, David
Jewell, Rosalyn
Kraatari-Tiri, Minna
Piard, Juliette
Coubes, Christine
Lam, Wayne
Lynch, Sally Ann
Groeschel, Samuel
Ramond, Francis
Fluss, Joël
Fagerberg, Christina
Brasch Andersen, Charlotte
Varvagiannis, Konstantinos
Kleefstra, Tjitske
Gérard, Bénédicte
Fradin, Mélanie
Vitobello, Antonio
Tenconi, Romano
Denommé-Pichon, Anne-Sophie
Vincent-Devulder, Aline
Haack, Tobias
Marsh, Joseph A
Laulund, Lone Walentin
Grimmel, Mona
Riess, Angelika
de Boer, Elke
Padilla-Lopez, Sergio
Bakhtiari, Somayeh
Ostendorf, Adam
Zweier, Christiane Gertrud  
Universitätsklinik für Humangenetik  
Smol, Thomas
Willems, Marjolaine
Faivre, Laurence
Scala, Marcello
Striano, Pasquale
Bagnasco, Irene
Koboldt, Daniel
Iascone, Maria
Suerink, Manon
Kruer, Michael C
Levy, Jonathan
Verloes, Alain
Abbott, Catherine M
Ruaud, Lyse
Additional Credits
Universitätsklinik für Humangenetik  
Journal
European journal of human genetics
Publisher
Springer Nature
ISSN
1476-5438
Access(Rights)
restricted
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