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- W3015280985 abstract "Muscle & NerveVolume 62, Issue 1 p. E44-E45 LETTER TO THE EDITOR A novel phenotype of hereditary spastic paraplegia type 7 associated with a compound heterozygous mutation in paraplegin Colin J. Mahoney PhD, MRCPI, Corresponding Author Colin J. Mahoney PhD, MRCPI colin.mahoney@sydney.edu.au orcid.org/0000-0002-5878-3859 Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia Correspondence Colin J. Mahoney PhD MRCPI, Brain and Mind Centre, Sydney Medical School, University of Sydney, 94 Mallett Street, Camperdown, Sydney, NSW 2050, Australia, Email: colin.mahoney@sydney.edu.auSearch for more papers by this authorThanuja Dharmadasa PhD, FRACP, Thanuja Dharmadasa PhD, FRACP Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorWilliam Huynh PhD, FRACP, William Huynh PhD, FRACP Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorJean-Pierre Halpern PhD, FRACP, Jean-Pierre Halpern PhD, FRACP Department of Neurology, Sydney Adventist Clinical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorSteve Vucic PhD, FRACP, Steve Vucic PhD, FRACP Department of Neurology, Westmead Hospital, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorDavid Mowat MBBS, FRACP, David Mowat MBBS, FRACP Centre for Clinical Genetics, Sydney Children's Hospital, Sydney, New South Wales, AustraliaSearch for more papers by this authorMatthew C. Kiernan DSc, FRACP, Matthew C. Kiernan DSc, FRACP Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this author Colin J. Mahoney PhD, MRCPI, Corresponding Author Colin J. Mahoney PhD, MRCPI colin.mahoney@sydney.edu.au orcid.org/0000-0002-5878-3859 Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia Correspondence Colin J. Mahoney PhD MRCPI, Brain and Mind Centre, Sydney Medical School, University of Sydney, 94 Mallett Street, Camperdown, Sydney, NSW 2050, Australia, Email: colin.mahoney@sydney.edu.auSearch for more papers by this authorThanuja Dharmadasa PhD, FRACP, Thanuja Dharmadasa PhD, FRACP Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorWilliam Huynh PhD, FRACP, William Huynh PhD, FRACP Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorJean-Pierre Halpern PhD, FRACP, Jean-Pierre Halpern PhD, FRACP Department of Neurology, Sydney Adventist Clinical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorSteve Vucic PhD, FRACP, Steve Vucic PhD, FRACP Department of Neurology, Westmead Hospital, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this authorDavid Mowat MBBS, FRACP, David Mowat MBBS, FRACP Centre for Clinical Genetics, Sydney Children's Hospital, Sydney, New South Wales, AustraliaSearch for more papers by this authorMatthew C. Kiernan DSc, FRACP, Matthew C. Kiernan DSc, FRACP Brain and Mind Centre, Sydney Medical School, University of Sydney, Sydney, New South Wales, AustraliaSearch for more papers by this author First published: 08 April 2020 https://doi.org/10.1002/mus.26882Citations: 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 Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume62, Issue1July 2020Pages E44-E45 RelatedInformation" @default.
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- W3015280985 title "A novel phenotype of hereditary spastic paraplegia type 7 associated with a compound heterozygous mutation in paraplegin" @default.
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