Novel RYR1 missense mutation causes core rod myopathy

Abstract

European Journal of NeurologyVolume 15, Issue 4 p. e31-e32 Novel RYR1 missense mutation causes core rod myopathy M. Von Der Hagen, M. Von Der Hagen Department of Pediatric Neurology, Technical University, Dresden, GermanySearch for more papers by this authorW. Kress, W. Kress Institute of Human Genetics, Julius- Maximilian University, WürzburgSearch for more papers by this authorG. Hahn, G. Hahn Department of Radiology, Technical University, DresdenSearch for more papers by this authorK. S. Brocke, K. S. Brocke Department of Pediatric Neurology, Technical University, Dresden, GermanySearch for more papers by this authorP. Mitzscherling, P. Mitzscherling Children’s Hospital, Technical University, DresdenSearch for more papers by this author A. Huebner, A. Huebner Children’s Hospital, Technical University, DresdenSearch for more papers by this authorC. Müller-Reible, C. Müller-Reible Institute of Human Genetics, Julius- Maximilian University, WürzburgSearch for more papers by this author G. Stoltenburg-Didinger, G. Stoltenburg-Didinger Departments of NeuropathologySearch for more papers by this author A. M. Kaindl, A. M. Kaindl Pediatric Neurology, Charité, Berlin, Germany Inserm U676-Paris 7, Paris, FranceSearch for more papers by this author M. Von Der Hagen, M. Von Der Hagen Department of Pediatric Neurology, Technical University, Dresden, GermanySearch for more papers by this authorW. Kress, W. Kress Institute of Human Genetics, Julius- Maximilian University, WürzburgSearch for more papers by this authorG. Hahn, G. Hahn Department of Radiology, Technical University, DresdenSearch for more papers by this authorK. S. Brocke, K. S. Brocke Department of Pediatric Neurology, Technical University, Dresden, GermanySearch for more papers by this authorP. Mitzscherling, P. Mitzscherling Children’s Hospital, Technical University, DresdenSearch for more papers by this author A. Huebner, A. Huebner Children’s Hospital, Technical University, DresdenSearch for more papers by this authorC. Müller-Reible, C. Müller-Reible Institute of Human Genetics, Julius- Maximilian University, WürzburgSearch for more papers by this author G. Stoltenburg-Didinger, G. Stoltenburg-Didinger Departments of NeuropathologySearch for more papers by this author A. M. Kaindl, A. M. Kaindl Pediatric Neurology, Charité, Berlin, Germany Inserm U676-Paris 7, Paris, FranceSearch for more papers by this author First published: 26 February 2008 https://doi.org/10.1111/j.1468-1331.2008.02094.xCitations: 16 Dr M. von der Hagen, Department of Pediatric Neurology, Technical University, Fetscherstr. 74, 01307 Dresden, Germany (tel.: +49 351 458 5456; fax: +40 351 458 5349; 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 No abstract is available for this article.Citing Literature Volume15, Issue4April 2008Pages e31-e32 RelatedInformation