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De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder
2017
107 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
3.58
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder | Researchclopedia
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Baylor College of Medicine
Jonas Denecke
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University Medical Center Hamburg-Eppendorf
Simon Edvardson
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Hadassah Medical Center
Estelle Colin
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Inserm
Alexander P.A. Stegmann
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Radboud University Nijmegen
Erica H. Gerkes
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University of Groningen
Marine Tessarech
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Université d'Angers
Dominique Bonneau
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Inserm
Magalie Barth
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Centre National de la Recherche Scientifique
Thomas Besnard
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Génétique Médicale & Génomique Fonctionelle
Benjamin Cogné
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Génétique Médicale & Génomique Fonctionelle
Anya Revah‐Politi
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Columbia University
Tim M. Strom
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Helmholtz Zentrum München
Jill A. Rosenfeld
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Baylor College of Medicine
Yaping Yang
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Baylor College of Medicine
Jennifer E. Posey
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Baylor College of Medicine
LaDonna Immken
Nelly Jouayed Oundjian
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Valley Hospital
Katherine L. Helbig
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Ambry Genetics (United States)
Naomi Meeks
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Children's Hospital Colorado
Kelsey Zegar
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University of Colorado Denver
Jenny Morton
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Birmingham Women’s and Children’s NHS Foundation Trust
Jolanda Schieving
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Radboud University Medical Center
Ana M. Claasen
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Translational Genomics Research Institute
Matthew J. Huentelman
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Translational Genomics Research Institute
Vinodh Narayanan
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Translational Genomics Research Institute
Keri Ramsey
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Translational Genomics Research Institute
Han G. Brunner
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Radboud University Nijmegen
Orly Elpeleg
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Hadassah Medical Center
Sandra Mercier
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Génétique Médicale & Génomique Fonctionelle
Stéphane Bezieau
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Génétique Médicale & Génomique Fonctionelle
Christian Kubisch
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University Medical Center Hamburg-Eppendorf
Tjitske Kleefstra
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Radboud University Nijmegen
Stefan Kindler
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Universität Hamburg
James R. Lupski
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Baylor College of Medicine
Hans‐Jürgen Kreienkamp
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Universität Hamburg