A gene (ETM) for essential tremor maps to chromosome 2p22-p25
We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Ob...
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Veröffentlicht in: | Movement disorders 1997-11, Vol.12 (6), p.859-864 |
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description | We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system. |
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Disord</addtitle><description>We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. These findings will facilitate the search for an ETM gene and may further our understanding of the human motor system.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Chromosome Aberrations - genetics</subject><subject>Chromosome Disorders</subject><subject>Chromosomes, Human, Pair 2 - genetics</subject><subject>Czech Republic - ethnology</subject><subject>Essential tremor</subject><subject>Genetic Linkage - genetics</subject><subject>Haplotypes - genetics</subject><subject>Human chromosome 2p</subject><subject>Humans</subject><subject>Linkage analysis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Nervous system as a whole</subject><subject>Neurology</subject><subject>Pedigree</subject><subject>Phenotype</subject><subject>Severity of Illness Index</subject><subject>Tremor - diagnosis</subject><subject>Tremor - genetics</subject><subject>Trinucleotide Repeats - genetics</subject><subject>United States</subject><subject>X Chromosome</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kL1LxEAQxRdR9PwoLYUUIlpEZ783hYX4DacWnlgum72JRpNL3M2h_vdGLhxWVgPzfvPm8QjZpXBMAdhJPY3HRgNloECukBGVnKaGSb1KRmCMTDk1coNsxvgGQKmkap2sZzzLGOgROT1LXnCGyeHl5O4oKZqQYIw460pXJV3Aul_Uro1J1yT-NTR1E5saE9YylrZMbpO1wlURd4a5RZ6uLifnN-n44fr2_Gycegl9gowLUMYxnHpApQ36HNGBEsJB5gvIC84cUzlqybQQIBTQXABH7QujpOZb5GDh24bmY46xs3UZPVaVm2Ezj1ZnQlEhTA-mC9CHJsaAhW1DWbvwbSnY37psX5dd1tXze4PxPK9xuqSHfnp9f9Bd9K4qgpv5Mi4xBlIJTXtML7DPssLv_3_au4vHvwGGwGXs8Gt56cK7VZpraZ_vr-0zvaeTi8nYav4DSFmOeg</recordid><startdate>199711</startdate><enddate>199711</enddate><creator>Higgins, Joseph J.</creator><creator>Pho, Lana T.</creator><creator>Nee, Linda E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>199711</creationdate><title>A gene (ETM) for essential tremor maps to chromosome 2p22-p25</title><author>Higgins, Joseph J. ; Pho, Lana T. ; Nee, Linda E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5085-934068a2edc0e678ecbeea0644a09cf0bf32a26be75274404601b403e7cf86573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Chromosome Aberrations - genetics</topic><topic>Chromosome Disorders</topic><topic>Chromosomes, Human, Pair 2 - genetics</topic><topic>Czech Republic - ethnology</topic><topic>Essential tremor</topic><topic>Genetic Linkage - genetics</topic><topic>Haplotypes - genetics</topic><topic>Human chromosome 2p</topic><topic>Humans</topic><topic>Linkage analysis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Nervous system as a whole</topic><topic>Neurology</topic><topic>Pedigree</topic><topic>Phenotype</topic><topic>Severity of Illness Index</topic><topic>Tremor - diagnosis</topic><topic>Tremor - genetics</topic><topic>Trinucleotide Repeats - genetics</topic><topic>United States</topic><topic>X Chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Higgins, Joseph J.</creatorcontrib><creatorcontrib>Pho, Lana T.</creatorcontrib><creatorcontrib>Nee, Linda E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Higgins, Joseph J.</au><au>Pho, Lana T.</au><au>Nee, Linda E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A gene (ETM) for essential tremor maps to chromosome 2p22-p25</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>1997-11</date><risdate>1997</risdate><volume>12</volume><issue>6</issue><spage>859</spage><epage>864</epage><pages>859-864</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>We report the results of linkage analysis in a large American family of Czech descent with dominantly inherited “Pure” essential tremor (ET) and genetic anticipation. Genetic loci on chromosome 2p22‐p25 establish linkage to this region with a maximum LOD score (Zmax) = 5.92 for the locus, D2S272. Obligate recombinant events place the ETM gene in a 15‐cM candidate interval between the genetic loci D2S168 and D2S224. Repeat expansion detection analysis suggests that expanded CAG trinucleotide sequences are associated with ET. 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subjects | Adolescent Adult Aged Biological and medical sciences Child Chromosome Aberrations - genetics Chromosome Disorders Chromosomes, Human, Pair 2 - genetics Czech Republic - ethnology Essential tremor Genetic Linkage - genetics Haplotypes - genetics Human chromosome 2p Humans Linkage analysis Medical sciences Middle Aged Nervous system (semeiology, syndromes) Nervous system as a whole Neurology Pedigree Phenotype Severity of Illness Index Tremor - diagnosis Tremor - genetics Trinucleotide Repeats - genetics United States X Chromosome |
title | A gene (ETM) for essential tremor maps to chromosome 2p22-p25 |
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