Atypical juvenile parkinsonism in a consanguineous SPG15 family
Identifieur interne : 002229 ( Istex/Corpus ); précédent : 002228; suivant : 002230Atypical juvenile parkinsonism in a consanguineous SPG15 family
Auteurs : Julia Schicks ; Matthis Synofzik ; Hjörvar Pétursson ; Johanna Huttenlocher ; Matthias Reimold ; Ludger Schöls ; Peter BauerSource :
- Movement Disorders [ 0885-3185 ] ; 2011-02-15.
Url:
DOI: 10.1002/mds.23472
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<caption>Supplementary figure: Pedigree showing segregation of the novel ZFYVE26 mutation. Black circles (women) and squares (men) indicate affected members. The genotypes are indicated below the analysed individuals.</caption>
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<noteGroup><note xml:id="fn2"><p>Relevant conflict of interest/financial disclosures: Nothing to Report. Full financial disclosures and author roles can be found in the online version of this article.</p>
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<titleInfo type="alternative" contentType="CDATA" lang="en"><title>Atypical juvenile parkinsonism in a consanguineous</title>
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<name type="personal"><namePart type="given">Julia</namePart>
<namePart type="family">Schicks</namePart>
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<affiliation>Department of Neurology Hertie‐Institute for Clinical Brain Research Tübingen, Germany</affiliation>
<affiliation>German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen Tübingen, Germany</affiliation>
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<name type="personal"><namePart type="given">Matthis</namePart>
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<affiliation>German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen Tübingen, Germany</affiliation>
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<name type="personal"><namePart type="given">Hjörvar</namePart>
<namePart type="family">Pétursson</namePart>
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<affiliation>Department of Medical Genetics Institute of Human Genetics University of Tübingen Tübingen, Germany</affiliation>
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<name type="personal"><namePart type="given">Johanna</namePart>
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<affiliation>Department of Nuclear Medicine University of Tübingen Tübingen, Germany</affiliation>
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<name type="personal"><namePart type="given">Ludger</namePart>
<namePart type="family">Schöls</namePart>
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<affiliation>Department of Neurology Hertie‐Institute for Clinical Brain Research Tübingen, Germany</affiliation>
<affiliation>German Centre of Neurodegenerative Diseases (DZNE), University of Tübingen Tübingen, Germany</affiliation>
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<name type="personal"><namePart type="given">Peter</namePart>
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<dateIssued encoding="w3cdtf">2011-02-15</dateIssued>
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<note type="content">*Relevant conflict of interest/financial disclosures: Nothing to Report. Full financial disclosures and author roles can be found in the online version of this article.</note>
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<note type="content"> Additional supporting information may be found in the online version of this article.Supporting Info Item: Supporting Information - Supporting Information Table - Supplementary figure: Pedigree showing segregation of the novel ZFYVE26 mutation. Black circles (women) and squares (men) indicate affected members. The genotypes are indicated below the analysed individuals. - Author Roles and Disclosures - </note>
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<identifier type="ISSN">0885-3185</identifier>
<identifier type="eISSN">1531-8257</identifier>
<identifier type="DOI">10.1002/(ISSN)1531-8257</identifier>
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<part><date>2011</date>
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