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A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathy.
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Document type | Article de périodique (Journal article) – Article de recherche |
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Access type | Accès restreint |
Publication date | 2012 |
Language | Anglais |
Journal information | "Archives of Neurology" - Vol. 69, no.7, p. 908-11 (2012) |
Peer reviewed | yes |
Publisher | American Medical Association ((United States) Chicago) |
issn | 0003-9942 |
e-issn | 1538-3687 |
Publication status | Publié |
Affiliation | UCL - SSS/DDUV - Institut de Duve |
MESH Subject | Administration, Oral ; Serine ; Adult ; Amino Acid Metabolism, Inborn Errors ; Charcot-Marie-Tooth Disease ; DNA Mutational Analysis ; Humans ; Male ; Metabolic Networks and Pathways ; Phosphoglycerate Dehydrogenase |
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Bibliographic reference | Méneret, Aurélie ; Wiame, Elsa ; Marelli, Cecilia ; Lenglet, Timothée ; Van Schaftingen, Emile ; et. al. A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathy.. In: Archives of Neurology, Vol. 69, no.7, p. 908-11 (2012) |
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Permanent URL | http://hdl.handle.net/2078.1/123563 |