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- W2016069141 abstract "Clinical GeneticsVolume 63, Issue 6 p. 456-457 Ion-ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN R S Devon, R S Devon Centre for Molecular Medicine and Therapeutics, 950 West 28th Avenue, Vancouver, BC, V6R 2L5, CanadaSearch for more papers by this author R S Devon, R S Devon Centre for Molecular Medicine and Therapeutics, 950 West 28th Avenue, Vancouver, BC, V6R 2L5, CanadaSearch for more papers by this author First published: 03 June 2003 https://doi.org/10.1034/j.1399-0004.2003.00095.x 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 Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 De Braekeleer M, Dallaire A, Mathieu J. Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in north-eastern Quebec. Hum Genet 1993: 91: 223 – 227. 2 Casaubon LK, Melanson M, Lopes-Cendes I et al. The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q. Am J Hum Genet 1996: 58: 28 – 34. Volume63, Issue6June 2003Pages 456-457 ReferencesRelatedInformation" @default.
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- W2016069141 title "Ion-ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN" @default.
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