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Konferensabstrakt2019

DTYMK deficiency is the cause of a novel vanishing brain disease

Vanoevelen, J. M.; Bierau, J.; Kamsteeg, E.; Wevers, R. A.; Bok, V. A.; van der Knaap, M.; Bugiani, M.; O'Driscoll, M.; van den Wijngaard, A.; Brunner, H. G.; Wang, L.; Stumpel, C. T. R. M.

Publicerad i

European Journal of Human Genetics
2019, Volym: 27, nummer: Supplement 2, sidor: 1095-1095
Utgivare: NATURE PUBLISHING GROUP

Konferens

52nd Conference of the European Society of Human Genetics (ESHG), JUN 15-18, 2019, Gothenburg, SWEDEN