Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

Journal: Nature Communications

Published: 2019-09-03

DOI: 10.1038/s41467-019-11951-x

Affiliations: 28

Authors: 37

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Institutions Share
Laboratory of Molecular Bases of Hereditary Kidney Diseases, Imagine Institute, France 0.27
Institute of Integrative Biology of the Cell (I2BC), France 0.12
Hôpital Necker-Enfants Malades, France 0.08
Hôpital Femme Mère Enfant (HFME), HCL, France 0.07
Department of Medicine (DoM), BCH, United States of America (USA) 0.05
Imagine Institute, France 0.05
Reference Centers for Rare Diseases, Imagine Institute, France 0.04
Structure Fédérative de Recherche Necker (SFR Necker), France 0.04
Institute of Chemistry of Natural Substances (ICSN), France 0.03
Bioinformatics Platform, Imagine Institute, France 0.03
Hôpital Purpan, CHU-Toulouse, France 0.03
Centre Hospitalier Universitaire de Lille (CHU Lille), France 0.03
Robert Debré University Hospital, France 0.03
UMC Utrecht Center for Molecular Medicine (CMM), Netherlands 0.03
UMC Department of Medical Genetics, Netherlands 0.03
Rambam Health Care Campus (RambamHCC), IIT, Israel 0.03
Toxicology Pharmacology and Cellular Signaling, France 0.01
Institute of Mineralogy, Materials Physics and Cosmochemistry (IMPMC), France 0.01
Laboratory of Genome Dynamics in the Immune System, Imagine Institute, France 0.01
Ligue Contre Le Cancer, France 0.01
Neuroimaging and Psychiatry, France 0.01

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