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G.P.91 A new syndrome characterized by demyelinating neuropathy and hydrocephalus caused by a heterozygous mutation in one of the aminoacyl-tRNA synthetase genes
by
Niks, E.H
,
Potjer, T.P
,
Al Momani, R
,
Sun, Y
,
Koot, R.W
,
van Dijk, J.G
,
Haring, D.A.J
,
Aten, E
,
Kriek, M
,
Santen, G.W.E
,
Lesnik Oberstein, S.A.M
Published in
Neuromuscular disorders : NMD
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Neuromuscular Disorders : Nmd
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Neurology
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