Genetic peroxisomal disorders: Why, when, and how to test
1998; Wiley; Volume: 44; Issue: 5 Linguagem: Inglês
10.1002/ana.410440502
ISSN1531-8249
AutoresHugo W. Moser, Gerald V. Raymond,
Tópico(s)RNA regulation and disease
ResumoAnnals of NeurologyVolume 44, Issue 5 p. 713-715 Editorial Genetic peroxisomal disorders: Why, when, and how to test Hugo W. Moser MD, Hugo W. Moser MD Department of Neurogenetics, Kennedy Krieger Institute and Departments of Neurology and Pediatrics, Johns Hopkins University, Baltimore, MDSearch for more papers by this authorGerald V. Raymond MD, Gerald V. Raymond MD Department of Neurogenetics, Kennedy Krieger Institute and Departments of Neurology and Pediatrics, Johns Hopkins University, Baltimore, MDSearch for more papers by this author Hugo W. Moser MD, Hugo W. Moser MD Department of Neurogenetics, Kennedy Krieger Institute and Departments of Neurology and Pediatrics, Johns Hopkins University, Baltimore, MDSearch for more papers by this authorGerald V. Raymond MD, Gerald V. Raymond MD Department of Neurogenetics, Kennedy Krieger Institute and Departments of Neurology and Pediatrics, Johns Hopkins University, Baltimore, MDSearch for more papers by this author First published: 08 October 2004 https://doi.org/10.1002/ana.410440502Citations: 9AboutPDF 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 Volume44, Issue5November 1998Pages 713-715 RelatedInformation
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