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Weterman, M.A.J.; Kuo, M.; Kenter, S.B.; Gordillo, S.; Karjosukarso, D.W.; Takase, R.; ... ; Baas, F.
2018
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities
Article / Letter to editor
metadata only
Barth, P.G.; Aronica, E.; Fox, S.; Fluiter, K.; Weterman, M.A.J.; Poretti, A.; ... ; Baas, F.
2017
Deregulated expression of EZH2 in congenital brainstem disconnection
Article / Letter to editor
open access
