Genome-wide scan for Parkinson's disease: The genePD Study
Identifieur interne : 000113 ( PascalFrancis/Curation ); précédent : 000112; suivant : 000114Genome-wide scan for Parkinson's disease: The genePD Study
Auteurs : A. L. Destefano [États-Unis] ; L. I. Golbe [États-Unis] ; M. H. Mark [États-Unis] ; A. M. Lazzarini [États-Unis] ; N. E. Maher [États-Unis] ; M. Saint-Hilaire [États-Unis] ; R. G. Feldman [États-Unis] ; M. Guttman [États-Unis] ; R. L. Watts [États-Unis] ; O. Suchowersky [Canada] ; A. L. Lafontaine [Canada] ; N. Labelle [Canada] ; M. F. Lew [États-Unis] ; C. H. Waters [États-Unis] ; J. H. Growdon [États-Unis] ; C. Singer [États-Unis] ; L. J. Currie [États-Unis] ; G. F. Wooten [États-Unis] ; P. Vieregge [Allemagne] ; P. P. Pramstaller [Italie] ; C. Klein [Allemagne] ; J. P. Hubble [États-Unis] ; M. Stacy [États-Unis] ; E. Montgomery [États-Unis] ; M. E. Macdonald [États-Unis] ; J. F. Gusella [États-Unis] ; R. H. Myers [États-Unis]Source :
- Neurology [ 0028-3878 ] ; 2001.
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Abstract
Article abstract-A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine β-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.
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<author><name sortKey="Klein, C" sort="Klein, C" uniqKey="Klein C" first="C." last="Klein">C. Klein</name>
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<author><name sortKey="Hubble, J P" sort="Hubble, J P" uniqKey="Hubble J" first="J. P." last="Hubble">J. P. Hubble</name>
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<author><name sortKey="Stacy, M" sort="Stacy, M" uniqKey="Stacy M" first="M." last="Stacy">M. Stacy</name>
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<author><name sortKey="Montgomery, E" sort="Montgomery, E" uniqKey="Montgomery E" first="E." last="Montgomery">E. Montgomery</name>
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<author><name sortKey="Gusella, J F" sort="Gusella, J F" uniqKey="Gusella J" first="J. F." last="Gusella">J. F. Gusella</name>
<affiliation wicri:level="1"><inist:fA14 i1="08"><s1>Department of Neurology, Massachusetts General Hospital, Harvard Medical School</s1>
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<author><name sortKey="Myers, R H" sort="Myers, R H" uniqKey="Myers R" first="R. H." last="Myers">R. H. Myers</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Boston University Schools of Medicine and of Public Health</s1>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Genome-wide scan for Parkinson's disease: The genePD Study</title>
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<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Department of Epidemiology and Biostatistics, Boston University Schools of Medicine and of Public Health</s1>
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<author><name sortKey="Golbe, L I" sort="Golbe, L I" uniqKey="Golbe L" first="L. I." last="Golbe">L. I. Golbe</name>
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<author><name sortKey="Mark, M H" sort="Mark, M H" uniqKey="Mark M" first="M. H." last="Mark">M. H. Mark</name>
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<author><name sortKey="Lazzarini, A M" sort="Lazzarini, A M" uniqKey="Lazzarini A" first="A. M." last="Lazzarini">A. M. Lazzarini</name>
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<author><name sortKey="Maher, N E" sort="Maher, N E" uniqKey="Maher N" first="N. E." last="Maher">N. E. Maher</name>
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<author><name sortKey="Saint Hilaire, M" sort="Saint Hilaire, M" uniqKey="Saint Hilaire M" first="M." last="Saint-Hilaire">M. Saint-Hilaire</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Boston University Schools of Medicine and of Public Health</s1>
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<author><name sortKey="Feldman, R G" sort="Feldman, R G" uniqKey="Feldman R" first="R. G." last="Feldman">R. G. Feldman</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Boston University Schools of Medicine and of Public Health</s1>
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<author><name sortKey="Guttman, M" sort="Guttman, M" uniqKey="Guttman M" first="M." last="Guttman">M. Guttman</name>
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<author><name sortKey="Watts, R L" sort="Watts, R L" uniqKey="Watts R" first="R. L." last="Watts">R. L. Watts</name>
<affiliation wicri:level="1"><inist:fA14 i1="05"><s1>Department of Neurology, Emory University School of Medicine</s1>
<s2>Atlanta, GA</s2>
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<author><name sortKey="Suchowersky, O" sort="Suchowersky, O" uniqKey="Suchowersky O" first="O." last="Suchowersky">O. Suchowersky</name>
<affiliation wicri:level="1"><inist:fA14 i1="06"><s1>Departments of Clinical Neurosciences and Medical Genetics, University of Calgary</s1>
<s2>Alberta</s2>
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<sZ>15 aut.</sZ>
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<author><name sortKey="Myers, R H" sort="Myers, R H" uniqKey="Myers R" first="R. H." last="Myers">R. H. Myers</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Department of Neurology, Boston University Schools of Medicine and of Public Health</s1>
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<series><title level="j" type="main">Neurology</title>
<title level="j" type="abbreviated">Neurology</title>
<idno type="ISSN">0028-3878</idno>
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<front><div type="abstract" xml:lang="en">Article abstract-A genome-wide scan for idiopathic PD in a sample of 113 PD-affected sibling pairs is reported. Suggestive evidence for linkage was found for chromosomes 1 (214 cM, lod = 1.20), 9 (136 cM, lod = 1.30), 10 (88 cM, lod = 1.07), and 16 (114 cM, lod = 0.93). The chromosome 9 region overlaps the genes for dopamine β-hydroxylase and torsion dystonia. Although no strong evidence for linkage was found for any locus, these results may be of value in comparison with similar studies by others.</div>
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<fA14 i1="12"><s1>Department of Neurology, General Regional Hospital Bolzano</s1>
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<fC07 i1="04" i2="X" l="SPA"><s0>Extrapiramidal síndrome</s0>
<s5>40</s5>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Maladie dégénérative</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="ENG"><s0>Degenerative disease</s0>
<s5>41</s5>
</fC07>
<fC07 i1="05" i2="X" l="SPA"><s0>Enfermedad degenerativa</s0>
<s5>41</s5>
</fC07>
<fC07 i1="06" i2="X" l="FRE"><s0>Génétique</s0>
<s5>45</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG"><s0>Genetics</s0>
<s5>45</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA"><s0>Genética</s0>
<s5>45</s5>
</fC07>
<fN21><s1>007</s1>
</fN21>
</pA>
</standard>
</inist>
</record>
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