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175 related items for PubMed ID: 19059613

  • 1. 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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  • 3. The neurology and natural history of patients with indeterminate CAG repeat length mutations of the Huntington disease gene.
    Panegyres PK, Goh JG.
    J Neurol Sci; 2011 Feb 15; 301(1-2):14-20. PubMed ID: 21147489
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  • 4. Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout.
    Magri S, Nanetti L, Mongelli A, Rizzo E, Taroni F, Mariotti C, Gellera C.
    Am J Med Genet A; 2021 Feb 15; 185(2):397-400. PubMed ID: 33247537
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  • 8. Juvenile onset Huntington disease resulting from a very large maternal expansion.
    Nahhas FA, Garbern J, Krajewski KM, Roa BB, Feldman GL.
    Am J Med Genet A; 2005 Sep 01; 137A(3):328-31. PubMed ID: 16096998
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  • 10. Normal CAG repeats in the Huntington gene in a family with benign familial chorea.
    Meszaros K, Brücke T, Fuchs K, Gerhard E, Sieghart W, vanDer Meer CH, Aschauer HN.
    Psychiatr Genet; 1996 Sep 01; 6(2):91-4. PubMed ID: 8840396
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  • 12. Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis.
    Jih KY, Lai KL, Lin KP, Liao YC, Lee YC.
    J Chin Med Assoc; 2023 Jan 01; 86(1):47-51. PubMed ID: 36599142
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  • 14. Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association study.
    Piras IS, Picinelli C, Iennaco R, Baccarin M, Castronovo P, Tomaiuolo P, Cucinotta F, Ricciardello A, Turriziani L, Nanetti L, Mariotti C, Gellera C, Lintas C, Sacco R, Zuccato C, Cattaneo E, Persico AM.
    Am J Med Genet B Neuropsychiatr Genet; 2020 Sep 01; 183(6):341-351. PubMed ID: 32652810
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  • 15. Exploring the correlates of intermediate CAG repeats in Huntington disease.
    Ha AD, Jankovic J.
    Postgrad Med; 2011 Sep 01; 123(5):116-21. PubMed ID: 21904093
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  • 17. Patients with features similar to Huntington's disease, without CAG expansion in huntingtin.
    Rosenblatt A, Ranen NG, Rubinsztein DC, Stine OC, Margolis RL, Wagster MV, Becher MW, Rosser AE, Leggo J, Hodges JR, ffrench-Constant CK, Sherr M, Franz ML, Abbott MH, Ross CA.
    Neurology; 1998 Jul 01; 51(1):215-20. PubMed ID: 9674805
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  • 19. Genetic features of Huntington disease in Cuban population: implications for phenotype, epidemiology and predictive testing.
    Vázquez-Mojena Y, Laguna-Salvia L, Laffita-Mesa JM, González-Zaldívar Y, Almaguer-Mederos LE, Rodríguez-Labrada R, Almaguer-Gotay D, Zayas-Feria P, Velázquez-Pérez L.
    J Neurol Sci; 2013 Dec 15; 335(1-2):101-4. PubMed ID: 24054538
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  • 20. 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 15; 87(2):167-72. PubMed ID: 24405192
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