A new syndrome characterized by demyelinating neuropathy and hydrocephalus caused by a heterozygous mutation in one of the aminoacyl-tRNA synthetase genes

Author(s):
Niks, E.H. (0000-0001-5892-5143); Potjer, T.P.; Momani, R. al; Sun, Y.; Koot, R.W.; Dijk, J.G. van; Haring, D.A.J.; Aten, E.; Kriek, M.; Santen, G.W.E.; Oberstein, S.A.M.L.
Published
2012
Publication type
Article / Letter to editor
Date issued
2012-10-31
Language
English
Is part of
hdl
1887/99534
doi
10.1016/j.nmd.2012.06.221