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- W2066798829 abstract "Movement DisordersVolume 24, Issue 16 p. 2428-2429 Letter to the Editor Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia† Coro Paisán-Ruiz PhD, Corresponding Author Coro Paisán-Ruiz PhD C.Paisan-Ruiz@ion.ucl.ac.uk Laboratory of Neurogenomics, Department of Molecular Neuroscience and Reta Lila Weston Laboratories, UCL Institute of Neurology, Queen Square, London, EnglandLaboratory of Neurogenomics, Department of Molecular Neuroscience and Reta Lila Weston Laboratories, UCL Institute of Neurology, Queen Square, London, EnglandSearch for more papers by this authorJavier Ruiz-Martinez MD, Javier Ruiz-Martinez MD Servicio de Neurología, Hospital Donostia-San Sebastián, Gipuzkoa, Spain, CIBERNED, SpainSearch for more papers by this authorMarta Ruibal MD, Marta Ruibal MD Servicio de Neurología, Hospital de Zumarraga, Gipuzkoa, SpainSearch for more papers by this authorKin Y. Mok MB, Kin Y. Mok MB Laboratory of Neurogenomics, Department of Molecular Neuroscience and Reta Lila Weston Laboratories, UCL Institute of Neurology, Queen Square, London, EnglandSearch for more papers by this authorBegona Indakoetxea MD, PhD, Begona Indakoetxea MD, PhD Servicio de Neurología, Hospital Donostia. San Sebastián, Gipuzkoa, SpainSearch for more papers by this authorAna Gorostidi PhD, Ana Gorostidi PhD Laboratorio de Neurogenetics, Hospital Donostia-San Sebastián, Gipuzkoa, SpainSearch for more papers by this authorJosé F. Martí Massó MD, PhD, José F. Martí Massó MD, PhD Servicio de Neurología, Hospital Donostia-San Sebastián, Gipuzkoa, SpainSearch for more papers by this author Coro Paisán-Ruiz PhD, Corresponding Author Coro Paisán-Ruiz PhD C.Paisan-Ruiz@ion.ucl.ac.uk Laboratory of Neurogenomics, Department of Molecular Neuroscience and Reta Lila Weston Laboratories, UCL Institute of Neurology, Queen Square, London, EnglandLaboratory of Neurogenomics, Department of Molecular Neuroscience and Reta Lila Weston Laboratories, UCL Institute of Neurology, Queen Square, London, EnglandSearch for more papers by this authorJavier Ruiz-Martinez MD, Javier Ruiz-Martinez MD Servicio de Neurología, Hospital Donostia-San Sebastián, Gipuzkoa, Spain, CIBERNED, SpainSearch for more papers by this authorMarta Ruibal MD, Marta Ruibal MD Servicio de Neurología, Hospital de Zumarraga, Gipuzkoa, SpainSearch for more papers by this authorKin Y. Mok MB, Kin Y. Mok MB Laboratory of Neurogenomics, Department of Molecular Neuroscience and Reta Lila Weston Laboratories, UCL Institute of Neurology, Queen Square, London, EnglandSearch for more papers by this authorBegona Indakoetxea MD, PhD, Begona Indakoetxea MD, PhD Servicio de Neurología, Hospital Donostia. San Sebastián, Gipuzkoa, SpainSearch for more papers by this authorAna Gorostidi PhD, Ana Gorostidi PhD Laboratorio de Neurogenetics, Hospital Donostia-San Sebastián, Gipuzkoa, SpainSearch for more papers by this authorJosé F. Martí Massó MD, PhD, José F. Martí Massó MD, PhD Servicio de Neurología, Hospital Donostia-San Sebastián, Gipuzkoa, SpainSearch for more papers by this author First published: 18 December 2009 https://doi.org/10.1002/mds.22849Citations: 27 † Potential conflict of interest: Nothing to report. 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 onFacebookTwitterLinked InRedditWechat Citing Literature Volume24, Issue1615 December 2009Pages 2428-2429 RelatedInformation" @default.
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- W2066798829 title "Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia" @default.
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