Glycocen storage disease type II: Genetic and biochemical analysis of novel mutations in infantile patients from Turkish ancestry
Publication year
1998Author(s)
Number of pages
7 p.
Source
Human Mutation, 11, 3, (1998), pp. 209-215ISSN
Publication type
Article / Letter to editor
Display more detailsDisplay less details
Organization
Paediatrics - OUD tm 2017
Journal title
Human Mutation
Volume
vol. 11
Issue
iss. 3
Page start
p. 209
Page end
p. 215
Subject
Inborn errors of metabolism; Erfelijke stofwisselingsziektenThis item appears in the following Collection(s)
- Academic publications [238441]
- Faculty of Medical Sciences [90373]
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