Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study

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Title:	Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
Author(s):	Nelis, E.; Broeckhoven, C. van; Mariman, E.C.M. ; Gabreëls-Festen, A.A.W.M.
Publication year:	1996
Source:	European Journal of Human Genetics, vol. 4, (1996), pp. 25-33
ISSN:	1018-4813
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/188335
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Subject:	Clinical description and delineation of genetic syndromes Pathogenesis of the hereditary neuropathies CMT1a and HNPP Klinische beschrijving en moleculaire definiëring van genetische syndromen Onderzoek naar de pathogenese van de hereditaire neuropathieen CMT1a en HNPP
Organization:	Human Genetics Neurology
Journal title:	European Journal of Human Genetics
Volume:	vol. 4
Page start:	p. 25
Page end:	p. 33