MOLECULAR AND CLINICAL CORRELATIONS IN SPINOCEREBELLAR ATAXIA TYPE-3 (SCA3) AND MACHADO-JOSEPH (MJD) DISEASE - EVIDENCE FOR MUTATIONS IN THE SAME GENE

被引:0
|
作者
MATILLA, T
KOSHY, B
MCCALL, A
CLARK, J
ZIEGLER, D
SUBRAMONY, SH
ZOGHBI, HY
机构
[1] BAYLOR COLL MED,HOUSTON,TX 77030
[2] UNIV KANSAS,KANSAS CITY,KS 66103
[3] UNIV MISSISSIPPI,MED CTR,JACKSON,MS 39216
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:101 / 101
页数:1
相关论文
共 50 条
  • [41] Machado-Joseph Disease spinocerebellar ataxia 3 responsive to buspirone
    Friedman, JH
    MOVEMENT DISORDERS, 1997, 12 (04) : 613 - 614
  • [42] Cambodian founder effect for spinocerebellar ataxia type 3 (Machado-Joseph disease)
    Jayadev, Suman
    Michelson, Sara
    Lipe, Hillary
    Bird, Thomas
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2006, 250 (1-2) : 110 - 113
  • [43] Chinese homozygous Machado–Joseph disease (MJD)/SCA3: a case report
    Sheng Zeng
    Junsheng Zeng
    Miao He
    Xianfeng Zeng
    Yao Zhou
    Zhen Liu
    Hong Jiang
    Beisha Tang
    Junling Wang
    Journal of Human Genetics, 2015, 60 : 157 - 160
  • [44] Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence
    Karina Carvalho Donis
    Jonas Alex Morales Saute
    Ana Carolina Krum-Santos
    Gabriel Vasata Furtado
    Eduardo Preusser Mattos
    Maria Luiza Saraiva-Pereira
    Vanessa Leotti Torman
    Laura Bannach Jardim
    neurogenetics, 2016, 17 : 107 - 113
  • [45] Conserved methyltransferase NSUN5: a novel genetic modifier of Machado-Joseph disease (MJD/SCA3)?
    Huang, M.
    Nibbeling, E.
    Vries, J. D.
    Brunt, E.
    Verschuuren-Bemelmans, C.
    Schmidt, T.
    Verbeek, D. S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 403 - 403
  • [46] Yemenite-Jewish families with Machado-Joseph disease (MJD/SCA3) share a recent common ancestor
    Sharony, Reuven
    Martins, Sandra
    Costa, Ines P. D.
    Zaltzman, Roy
    Amorim, Antonio
    Sequeiros, Jorge
    Gordon, Carlos R.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 (11) : 1731 - 1737
  • [47] Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives
    Cecchin, C. R.
    Pires, A. P.
    Rieder, C. R.
    Monte, T. L.
    Silveira, I.
    Carvalho, T.
    Saraiva-Pereira, M. L.
    Sequeiros, J.
    Jardim, L. B.
    COMMUNITY GENETICS, 2007, 10 (01) : 19 - 26
  • [48] Machado-Joseph disease/SCA3 and myotonic dystrophy type 1 in a single patient
    Miura, Shiroh
    Ohyagi, Yasumasa
    Miike, Taro
    Noda, Kazuhito
    Motomura, Kyoko
    Ayabe, Mitsuyoshi
    Aizawa, Hisamichi
    Taniwaki, Takayuki
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2009, 111 (10) : 791 - 794
  • [49] Repeated mesenchymal stromal cells treatment sustainably alleviates Machado-Joseph disease/spinocerebellar ataxia type-3
    Miranda, C. O.
    Marcelo, A.
    Silva, T. P.
    Barata, J.
    Vasconcelos-Ferreira, A.
    Pereira, D.
    Duarte, S.
    Nobrega, C.
    Sereno, J.
    Petrella, L.
    Paiva, V. H.
    Castelhano, J.
    Nobre, R. J.
    Gomes, C.
    Castelo-Branco, M.
    Pereira de Almeida, L.
    HUMAN GENE THERAPY, 2018, 29 (12) : A56 - A56
  • [50] Genomic structure of the human Machado-Joseph disease (MJD/SCA3) locus on chromosome 14q32.1.
    Sell, C
    Cemal, C
    Chamberlain, S
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A419 - A419