Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
Christelle Arrondel(Délégation Paris 5), Géraldine Mollet(Inserm), Justine Bacchetta(Université Claude Bernard Lyon 1), Bruno Collinet(Université Paris-Sud), Ewen Lescop(Université Paris-Sud), Gaëlle Martin(Inserm), Herman van Tilbeurgh(Université Paris-Sud), Patrick Revy(Inserm), Daniela A. Braun(University Hospital Münster), D. Durand, Fabien Névo(Inserm), Sophie Collardeau‐Frachon(Université Claude Bernard Lyon 1), Nathalie Boddaert(St Nicholas Hospital), Laurine Buscara(Inserm), Cécile Masson(Délégation Paris 5), Sylvia Sanquer(Hôpital Necker-Enfants Malades), Olivier Gribouval(Inserm), Bruno Ranchin(Hospices Civils de Lyon), Sophia Missoury(Université Paris-Sud), Dominique Liger(Université Paris-Sud), Corinne Antignac(Hôpital Necker-Enfants Malades), Mélanie Parisot(Institut des Maladies Génétiques Imagine), Albertien M. van Eerde(Hospital Reina Sofía de Murcia), Giulia Menara(Inserm), Stéphane Decramer(Inserm), Anne‐Claire Boschat(Inserm), Friedhelm Hildebrandt(Boston Children's Hospital), Robert Novo(Hôpital Jeanne de Flandre), Ida Chiara Guerrera(Centre National de la Recherche Scientifique), Olivia Boyer(Hôpital Necker-Enfants Malades), Rozemarijn Snoek(University Medical Center Utrecht), Audrey Laurent(Université Claude Bernard Lyon 1), Daniella Magen(Technion – Israel Institute of Technology), Marie-Alice Macher(Assistance Publique – Hôpitaux de Paris), Marina Charbit(Hôpital Necker-Enfants Malades), Eduardo Machuca(Inserm), Julie Patat(Délégation Paris 5)
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