Title: X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy
Abstract: Journal of the Peripheral Nervous SystemVolume 16, Issue 4 p. 353-355 X-linked adrenomyeloneuropathy due to a novel missense mutation in the ABCD1 start codon presenting as demyelinating neuropathy Marc Engelen, Marc Engelen Department of Neurology Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorAnneke J. van der Kooi, Anneke J. van der Kooi Department of NeurologySearch for more papers by this authorStephan Kemp, Stephan Kemp Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorRonald J. A. Wanders, Ronald J. A. Wanders Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorErik A. Sistermans, Erik A. Sistermans Department of Clinical Genetics, VU Medical Centre, AmsterdamSearch for more papers by this authorHans R. Waterham, Hans R. Waterham Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorJohannes T. M. Koelman, Johannes T. M. Koelman Department of NeurologySearch for more papers by this authorBjörn M. van Geel, Björn M. van Geel Department of Neurology Department of Neurology, Medical Center Alkmaar, Alkmaar, The NetherlandsSearch for more papers by this authorMarianne de Visser, Marianne de Visser Department of NeurologySearch for more papers by this author Marc Engelen, Marc Engelen Department of Neurology Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorAnneke J. van der Kooi, Anneke J. van der Kooi Department of NeurologySearch for more papers by this authorStephan Kemp, Stephan Kemp Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorRonald J. A. Wanders, Ronald J. A. Wanders Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorErik A. Sistermans, Erik A. Sistermans Department of Clinical Genetics, VU Medical Centre, AmsterdamSearch for more papers by this authorHans R. Waterham, Hans R. Waterham Laboratory Genetic Metabolic Diseases, Academic Medical Center, AmsterdamSearch for more papers by this authorJohannes T. M. Koelman, Johannes T. M. Koelman Department of NeurologySearch for more papers by this authorBjörn M. van Geel, Björn M. van Geel Department of Neurology Department of Neurology, Medical Center Alkmaar, Alkmaar, The NetherlandsSearch for more papers by this authorMarianne de Visser, Marianne de Visser Department of NeurologySearch for more papers by this author First published: 16 December 2011 https://doi.org/10.1111/j.1529-8027.2011.00367.xCitations: 6 Dr. Marianne de Visser, Department of Neurology, Academic Medical Center, Meibergdreef 9, P.O. Box 22600, Amsterdam, The Netherlands. Tel: +31 20 5663445; Fax: +31-205669374; E-mail: [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Citing Literature Volume16, Issue4December 2011Pages 353-355 RelatedInformation
Publication Year: 2011
Publication Date: 2011-12-01
Language: en
Type: letter
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 8
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