Rapid diagnosis and methionine administration: basis for a favourable outcome in a patient with methylenetetrahydrofolate reductase deficiency.
Publication year
1999Author(s)
Number of pages
3 p.
Source
Journal of Inherited Metabolic Disease, 22, (1999), pp. 240-242ISSN
Publication type
Article / Letter to editor
Display more detailsDisplay less details
Organization
Paediatrics - OUD tm 2017
Neurology
Journal title
Journal of Inherited Metabolic Disease
Volume
vol. 22
Page start
p. 240
Page end
p. 242
Subject
Enzymatic and molecular genetic defects causing hyperhomocysteinemia; Enzymatische en moleculair genetische defecten als oorzaak voor hyperhomocysteinemia; Neuromusculaire en neurometabole ziektenThis item appears in the following Collection(s)
- Academic publications [243908]
- Faculty of Medical Sciences [92803]
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