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Defects in t6A tRNA modification due to GON7 and YRDC mutat..:
Arrondel, Christelle, C
;
Missoury, Sophia
;
Snoek, Rozemarijn
...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-019-11951-x. , 2019
Link:
https://inserm.hal.science/inserm-02322309
RT Journal T1
Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftinserm:oai:HAL:inserm-02322309v1&Exemplar=1&LAN=DE A1 Arrondel, Christelle, C A1 Missoury, Sophia A1 Snoek, Rozemarijn A1 Patat, Julie A1 Menara, Giulia A1 Collinet, Bruno A1 Liger, Dominique A1 Durand, Dominique A1 Gribouval, Olivier A1 Boyer, Olivia A1 Buscara, Laurine A1 Martin, Gaëlle A1 Machuca, Eduardo A1 Nevo, Fabien A1 Lescop, Ewen A1 Braun, Daniela A1 Boschat, Anne-Claire A1 Sanquer, Sylvia A1 Guerrera, Ida Chiara A1 Revy, Patrick A1 Parisot, Mélanie A1 Masson, Cécile A1 Boddaert, Nathalie A1 Charbit, Marina A1 Decramer, Stéphane A1 Novo, Robert A1 Macher, Marie-Alice A1 Ranchin, Bruno A1 Bacchetta, Justine A1 Laurent, Audrey A1 Collardeau-Frachon, Sophie A1 van Eerde, Albertien, M A1 Hildebrandt, Friedhelm A1 Magen, Daniella A1 Antignac, Corinne A1 van Tilbeurgh, Herman A1 Mollet, Geraldine PB HAL CCSD; Nature Publishing Group YR 2019 K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-019-11951-x LK http://dx.doi.org/https://inserm.hal.science/inserm-02322309 DO https://inserm.hal.science/inserm-02322309 SF ELIB - SuUB Bremen
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