PUBLICATIONS
- Arrondel, C., Missoury, S., Snoek, R., Patat, J., Menara, G., Collinet, B., Liger, D., Durand, D., Gribouval, O., Boyer, O., Buscara, L., Martin, G., Machuca, E., Nevo, F., Lescop, E., Braun, D.A., Boschat, A.C., Sanquer, S., Guerrera, I.C., Revy, P., Parisot, M., Masson, C., Boddaert, N., Charbit, M., Decramer, S., Novo, R., Macher, M.A., Ranchin, B., Bacchetta, J., Laurent, A., Collardeau-Frachon, S., van Eerde, A.M., Hildebrandt, F., Magen, D., Antignac, C., van Tilbeurgh, H., Mollet, G. "Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome" Nature Communications., 10: art.n° 3967. (2019).