Abstract
American Journal of Medical GeneticsVolume 109, Issue 3 p. 246-246 Correspondence SMN2 deletion in childhood-onset spinal muscular atrophy J.M. Cobben, Corresponding Author J.M. Cobben [email protected] Department of Clinical Genetics, Free University Medical Centre, Amsterdam, The NetherlandsClinical Geneticist, Department of Clinical Genetics, Free University Medical Centre, De Boelelaan 1117, 1007 MB Amsterdam, The Netherlands.Search for more papers by this authorM. de Visser, M. de Visser Department of Neurology, Academic Medical Centre, Amsterdam, The NetherlandsSearch for more papers by this author J.M. Cobben, Corresponding Author J.M. Cobben [email protected] Department of Clinical Genetics, Free University Medical Centre, Amsterdam, The NetherlandsClinical Geneticist, Department of Clinical Genetics, Free University Medical Centre, De Boelelaan 1117, 1007 MB Amsterdam, The Netherlands.Search for more papers by this authorM. de Visser, M. de Visser Department of Neurology, Academic Medical Centre, Amsterdam, The NetherlandsSearch for more papers by this author First published: 14 March 2002 https://doi.org/10.1002/ajmg.10354Citations: 1Read 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 Volume109, Issue31 May 2002Pages 246-246 RelatedInformation
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