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Journal Abstract Search

248 related items for PubMed ID: 11807410

  • 1. Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases?
    Savić D, Topisirović I, Keckarević M, Keckarević D, Major T, Culjković B, Stojković O, Rakocević-Stojanović V, Mladenović J, Todorović S, Apostolski S, Romac S.
    Psychiatr Genet; 2001 Dec; 11(4):201-5. PubMed ID: 11807410
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  • 2. No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3.
    Hellenbroich Y, Kaulich M, Opitz S, Schwinger E, Zühlke C.
    Psychiatr Genet; 2004 Jun; 14(2):61-3. PubMed ID: 15167689
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  • 7. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group.
    Pujana MA, Corral J, Gratacòs M, Combarros O, Berciano J, Genís D, Banchs I, Estivill X, Volpini V.
    Hum Genet; 1999 Jun; 104(6):516-22. PubMed ID: 10453742
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  • 8. [Analysis and application of SCA1 and SCA3/MJD gene CAG repeats in Han population in Northeastern China].
    Jiang M, Jin CL, Lin CK, Qiu GR, Liu ZL, Wang CX, Sun KL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):83-5. PubMed ID: 14767919
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  • 9. Imperfect CAG repeats form diverse structures in SCA1 transcripts.
    Sobczak K, Krzyzosiak WJ.
    J Biol Chem; 2004 Oct 01; 279(40):41563-72. PubMed ID: 15292212
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  • 11. The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with Huntington disease and healthy controls.
    Keckarevic D, Culjkovic B, Savic D, Stojkovic O, Kostic V, Vukosavic S, Romac S.
    J Neurogenet; 2000 Dec 01; 14(4):257-63. PubMed ID: 11342385
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  • 16. [Studies on the CAG repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese Han].
    Wang J, Xu Q, Lei L, Shen L, Jiang H, Li X, Zhou Y, Yi J, Zhou J, Yan X, Pan Q, Xia K, Tang B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Dec 01; 26(6):620-5. PubMed ID: 19953482
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  • 20. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ, Zhang BR, Wu DW, Tian J, Zhang H.
    Yi Chuan; 2007 Jun 01; 29(6):688-92. PubMed ID: 17650485
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