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Journal Abstract Search

132 related items for PubMed ID: 24405192

  • 1. Founder mutation for Huntington disease in Caucasus Jews.
    Melamed O, Behar DM, Bram C, Magal N, Pras E, Reznik-Wolf H, Borochowitz ZU, Davidov B, Mor-Cohen R, Baris HN.
    Clin Genet; 2015 Feb; 87(2):167-72. PubMed ID: 24405192
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  • 2. Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and Karaites.
    Zitser J, Thaler A, Inbar N, Gad A, Faust-Socher A, Paleacu D, Anca-Herschkovitch M, Balash Y, Shabtai H, Ash EL, Merkin L, Manor Y, Kestenbaum M, Bar David A, Peretz C, Naiman T, Bar-Shira A, Orr-Urtreger A, Dangoor N, Giladi N, Gurevich T.
    Neurodegener Dis; 2017 Feb; 17(6):281-285. PubMed ID: 28848105
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  • 5. Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene: Huntington disease or phenocopy?
    Herishanu YO, Parvari R, Pollack Y, Shelef I, Marom B, Martino T, Cannella M, Squitieri F.
    J Neurol Sci; 2009 Feb 15; 277(1-2):143-6. PubMed ID: 19059613
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  • 7. Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
    García-Planells J, Burguera JA, Solís P, Millán JM, Ginestar D, Palau F, Espinós C.
    Hum Mutat; 2005 May 15; 25(5):453-9. PubMed ID: 15832309
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  • 9. Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology.
    Uhlmann WR, Peñaherrera MS, Robinson WP, Milunsky JM, Nicholson JM, Albin RL.
    Am J Med Genet A; 2015 May 15; 167A(5):1152-60. PubMed ID: 25736541
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  • 10. The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.
    Kay C, Tirado-Hurtado I, Cornejo-Olivas M, Collins JA, Wright G, Inca-Martinez M, Veliz-Otani D, Ketelaar ME, Slama RA, Ross CJ, Mazzetti P, Hayden MR.
    Eur J Hum Genet; 2017 Feb 15; 25(3):332-340. PubMed ID: 28000697
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  • 11. The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.
    Kay C, Collins JA, Wright GEB, Baine F, Miedzybrodzka Z, Aminkeng F, Semaka AJ, McDonald C, Davidson M, Madore SJ, Gordon ES, Gerry NP, Cornejo-Olivas M, Squitieri F, Tishkoff S, Greenberg JL, Krause A, Hayden MR.
    Am J Med Genet B Neuropsychiatr Genet; 2018 Apr 15; 177(3):346-357. PubMed ID: 29460498
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  • 12. CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup.
    Warby SC, Montpetit A, Hayden AR, Carroll JB, Butland SL, Visscher H, Collins JA, Semaka A, Hudson TJ, Hayden MR.
    Am J Hum Genet; 2009 Mar 15; 84(3):351-66. PubMed ID: 19249009
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  • 18. The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation.
    Costa MDC, Magalhães P, Guimarães L, Maciel P, Sequeiros J, Sousa A.
    J Hum Genet; 2006 Mar 15; 51(3):189-195. PubMed ID: 16372132
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