Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion

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Publication year
2012
Author(s)
Voermans, N.C.
Kleefstra, T.
Gabreels-Festen, A.A.
Faas, B.H.
Kamsteeg, E.J.
Houlden, H.
Laura, M.
Polke, J.M.
Pandraud, A.
van Ruissen, F.
Engelen, B.G.M. van
Reilly, M.M.
Source
Journal of the Peripheral Nervous System, 17, 2, (2012), pp. 223-5
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/109505   https://hdl.handle.net/2066/109505
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