A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1

被引：13
|
作者：
Valdmanis, PN
Lopes, AAS
Gros-Louis, F
Stewart, JD
Rouleau, GA
Dupré, N
机构：
[1] McGill Univ, Ctr Hlth, Res Inst, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Ctr Res Neurosci, Montreal, PQ H3G 1A4, Canada
[3] Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2B4, Canada
[4] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[5] Univ Laval, Dept Neurol Sci, Ctr Rech, Ctr Hosp Affilie,Hop Enfant Jesus, Quebec City, PQ G1J 1Z4, Canada
来源：
JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 08期
关键词：
D O I：
10.1136/jmg.2004.019711
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
[No abstract available]
引用
收藏
页码：634 / 639
页数：6
相关论文
共 7 条
  • [1] Autosomal dominant sensory ataxia, a new disease entity, maps to chromosome 8q11.23-8p12.1
    Valdmanis, PN
    Brunet, D
    Weston, L
    Rouleau, GA
    Dupre, N
    NEUROLOGY, 2006, 66 (05) : 278 - 278
  • [2] A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1
    Funayama, M
    Hasegawa, K
    Kowa, H
    Saito, M
    Tsuji, S
    Obata, F
    ANNALS OF NEUROLOGY, 2002, 51 (03) : 296 - 301
  • [3] A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3
    Hanein, Sylvain
    Duerr, Alexandra
    Ribai, Pascale
    Forlani, Sylvie
    Leutenegger, Anne-Louise
    Nelson, Isabelle
    Babron, Marie-Claude
    Elleuch, Nizar
    Depienne, Christel
    Charon, Celine
    Brice, Alexis
    Stevanin, Giovanni
    HUMAN GENETICS, 2007, 122 (3-4) : 261 - 273
  • [4] A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3
    Sylvain Hanein
    Alexandra Dürr
    Pascale Ribai
    Sylvie Forlani
    Anne-Louise Leutenegger
    Isabelle Nelson
    Marie-Claude Babron
    Nizar Elleuch
    Christel Depienne
    Céline Charon
    Alexis Brice
    Giovanni Stevanin
    Human Genetics, 2007, 122 : 261 - 273
  • [5] A new locus for autosomal recessive cone-rod dystrophy maps to Chromosome 8p12-q11 distal to RP1.
    Danciger, M
    Inglehearn, CF
    Lyon, JE
    Jacobson, SG
    Farber, DB
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 309 - 309
  • [6] Chromosome 13 breakpoints in the t(8;13) (p11;q12) are tightly clustered and are associated with a novel gene.
    Reiter, A
    Sohal, J
    Chase, A
    Macdonald, DHC
    Aguiar, RCT
    Goncalves, C
    Hernandez, JM
    Goldman, JM
    Cross, NCP
    BLOOD, 1997, 90 (10) : 1422 - 1422
  • [7] Identification of a novel gene, 4P11, which maps to the D142H8 region of chromosome 21q22.1 and is closely linked to the IFN-γ receptor-2 (AF-1) gene.
    Bradshaw, G
    Cook, JR
    Donnelly, RJ
    Pestka, S
    EUROPEAN CYTOKINE NETWORK, 1998, 9 (03) : 504 - 504
1