Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
Publication year
1996Source
European Journal of Human Genetics, 4, (1996), pp. 25-33ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Neurology
Journal title
European Journal of Human Genetics
Volume
vol. 4
Page start
p. 25
Page end
p. 33
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 HNPPThis item appears in the following Collection(s)
- Academic publications [204024]
- Faculty of Medical Sciences [80459]
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