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The R98Q variation in DJ-1 represents a rare polymorphism

2003; Wiley; Volume: 55; Issue: 1 Linguagem: Inglês

10.1002/ana.10816

ISSN

1531-8249

Autores

Katja Hedrich, Nora Schäfer, Robert Hering, Johann Hagenah, Andrea Judith Lanthaler, E. Schwinger, Patricia L. Kramer, Laurie J. Ozelius, Susan Bressman, Giovanni Abbruzzese, Paolo Martinelli, Vladimir Kostić, Peter P. Pramstaller, P. Vieregge, Olaf Rieß, Christine Klein,

Tópico(s)

Genetics and Neurodevelopmental Disorders

Resumo

Annals of NeurologyVolume 55, Issue 1 p. 145-145 Letters The R98Q variation in DJ-1 represents a rare polymorphism Katja Hedrich PhD, Katja Hedrich PhD Department of Neurology, University of Lübeck, Lübeck Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorNora Schäfer BS, Nora Schäfer BS Department of Neurology, University of Lübeck, Lübeck Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorRobert Hering PhD, Robert Hering PhD Department of Medical Genetics, University of Tübingen, Tübingen, GermanySearch for more papers by this authorJohann Hagenah MD, Johann Hagenah MD Department of Neurology, University of Lübeck, LübeckSearch for more papers by this authorAndrea J. Lanthaler MA, Andrea J. Lanthaler MA Department of Hematology, Regional General Hospital, Bolzano, ItalySearch for more papers by this authorEberhard Schwinger MD, Eberhard Schwinger MD Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorPatricia L. Kramer PhD, Patricia L. Kramer PhD Department of Neurology, Oregon Health Sciences University, Portland, ORSearch for more papers by this authorLaurie J. Ozelius PhD, Laurie J. Ozelius PhD Department of Molecular Genetics, Albert Einstein College of Medicine, BronxSearch for more papers by this authorSusan B. Bressman MD, Susan B. Bressman MD Department of Neurology, Beth Israel Medical Center, New York, NYSearch for more papers by this authorGiovanni Abbruzzese MD, Giovanni Abbruzzese MD Department of Neurological Sciences and Vision, University of Genova, GenovaSearch for more papers by this authorPaolo Martinelli MD, Paolo Martinelli MD Department of Neurological Sciences, University of Bologna, Bologna, ItalySearch for more papers by this authorVladimir Kostic MD, Vladimir Kostic MD Department of Neurology, School of Medicine, University of Belgrade, Belgrade, SerbiaSearch for more papers by this authorPeter P. Pramstaller MD, Peter P. Pramstaller MD Department of Neurology, Regional General Hospital, and EURAC-Research, Genetic Medicine, Bolzano, ItalySearch for more papers by this authorPeter Vieregge MD, Peter Vieregge MD Department of Neurology, University of Lübeck, Lübeck Hospital of Lippe-Lemgo, Lemgo, GermanySearch for more papers by this authorOlaf Riess PhD, Olaf Riess PhD Department of Medical Genetics, University of Tübingen, Tübingen, GermanySearch for more papers by this authorChristine Klein MD, Christine Klein MD Department of Neurology, University of Lübeck, Lübeck Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this author Katja Hedrich PhD, Katja Hedrich PhD Department of Neurology, University of Lübeck, Lübeck Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorNora Schäfer BS, Nora Schäfer BS Department of Neurology, University of Lübeck, Lübeck Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorRobert Hering PhD, Robert Hering PhD Department of Medical Genetics, University of Tübingen, Tübingen, GermanySearch for more papers by this authorJohann Hagenah MD, Johann Hagenah MD Department of Neurology, University of Lübeck, LübeckSearch for more papers by this authorAndrea J. Lanthaler MA, Andrea J. Lanthaler MA Department of Hematology, Regional General Hospital, Bolzano, ItalySearch for more papers by this authorEberhard Schwinger MD, Eberhard Schwinger MD Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this authorPatricia L. Kramer PhD, Patricia L. Kramer PhD Department of Neurology, Oregon Health Sciences University, Portland, ORSearch for more papers by this authorLaurie J. Ozelius PhD, Laurie J. Ozelius PhD Department of Molecular Genetics, Albert Einstein College of Medicine, BronxSearch for more papers by this authorSusan B. Bressman MD, Susan B. Bressman MD Department of Neurology, Beth Israel Medical Center, New York, NYSearch for more papers by this authorGiovanni Abbruzzese MD, Giovanni Abbruzzese MD Department of Neurological Sciences and Vision, University of Genova, GenovaSearch for more papers by this authorPaolo Martinelli MD, Paolo Martinelli MD Department of Neurological Sciences, University of Bologna, Bologna, ItalySearch for more papers by this authorVladimir Kostic MD, Vladimir Kostic MD Department of Neurology, School of Medicine, University of Belgrade, Belgrade, SerbiaSearch for more papers by this authorPeter P. Pramstaller MD, Peter P. Pramstaller MD Department of Neurology, Regional General Hospital, and EURAC-Research, Genetic Medicine, Bolzano, ItalySearch for more papers by this authorPeter Vieregge MD, Peter Vieregge MD Department of Neurology, University of Lübeck, Lübeck Hospital of Lippe-Lemgo, Lemgo, GermanySearch for more papers by this authorOlaf Riess PhD, Olaf Riess PhD Department of Medical Genetics, University of Tübingen, Tübingen, GermanySearch for more papers by this authorChristine Klein MD, Christine Klein MD Department of Neurology, University of Lübeck, Lübeck Department of Human Genetics, University of Lübeck, LübeckSearch for more papers by this author First published: 30 December 2003 https://doi.org/10.1002/ana.10816Citations: 17Read 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 References 1 Hague S, Rogaeva E, Hernandez D, et al. Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation. Ann Neurol 2003; 54: 271– 274. 2 Bonifati V, Rizzu P, van Baren MJ, et al. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science 2003; 299: 256– 259. 3 Passarge E. Color atlas of genetics. New York: Thieme Medical Publishers, 1995. Citing Literature Volume55, Issue1January 2004Pages 145-145 ReferencesRelatedInformation

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