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• W2034654615 abstract "Clinical GeneticsVolume 81, Issue 6 p. 602-604 Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion NM Allen, Corresponding Author NM Allen Department of Pediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Temple Street, Dublin 1, IrelandDr Nicholas Mark AllenDepartment of Neurology and Clinical NeurophysiologyChildren's University Hospital,Temple Street Dublin 1, IrelandTel.: +353 (0)1 8784200Fax: +353 (0)1 8784444e-mail: nicholasallen@physicians.ieSearch for more papers by this authorB O’hIci, B O’hIci National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin 12, IrelandSearch for more papers by this authorG Anderson, G Anderson Department of Histopathology, Great Ormond Street Hospital for Children, London, UKSearch for more papers by this authorT Nestor, T Nestor Department of Pediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Temple Street, Dublin 1, IrelandSearch for more papers by this authorS Ann Lynch, S Ann Lynch National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin 12, IrelandSearch for more papers by this authorMD King, MD King Department of Pediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Temple Street, Dublin 1, IrelandSearch for more papers by this author NM Allen, Corresponding Author NM Allen Department of Pediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Temple Street, Dublin 1, IrelandDr Nicholas Mark AllenDepartment of Neurology and Clinical NeurophysiologyChildren's University Hospital,Temple Street Dublin 1, IrelandTel.: +353 (0)1 8784200Fax: +353 (0)1 8784444e-mail: nicholasallen@physicians.ieSearch for more papers by this authorB O’hIci, B O’hIci National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin 12, IrelandSearch for more papers by this authorG Anderson, G Anderson Department of Histopathology, Great Ormond Street Hospital for Children, London, UKSearch for more papers by this authorT Nestor, T Nestor Department of Pediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Temple Street, Dublin 1, IrelandSearch for more papers by this authorS Ann Lynch, S Ann Lynch National Centre for Medical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin 12, IrelandSearch for more papers by this authorMD King, MD King Department of Pediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Temple Street, Dublin 1, IrelandSearch for more papers by this author First published: 28 December 2011 https://doi.org/10.1111/j.1399-0004.2011.01777.xCitations: 15Read 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 onFacebookTwitterLinked InRedditWechat Citing Literature Volume81, Issue6June 2012Pages 602-604 RelatedInformation" @default.
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• W2034654615 title "Variant late-infantile neuronal ceroid lipofuscinosis due to a novel heterozygous CLN8 mutation and de novo 8p23.3 deletion" @default.
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