AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA (SCA) IN A SIBERIAN FOUNDER POPULATION - ASSIGNMENT TO THE SCA1 LOCUS

被引:12
|
作者
LUNKES, A [1 ]
GOLDFARB, LG [1 ]
PLATONOV, FA [1 ]
ALEXEEV, VP [1 ]
DUENASBARAJAS, E [1 ]
GAJDUSEK, DC [1 ]
AUBURGER, G [1 ]
机构
[1] NINCDS, BETHESDA, MD 20892 USA
关键词
D O I
10.1006/exnr.1994.1070
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In seven families from a Siberian founder population with autosomal dominant spinocerebellar ataxia (SCA) genetic analysis of the polymorphisms flanking the SCA1 locus on chromosome 6p showed allelic association with disease inheritance. While the association was absolute in the case of microsatellite D6S274, an allele switch was observed for D6S89 in two families, suggesting a historic recombinant. Further genetic and physical study of this recombinant event could be instrumental for the precise localization and identification of the SCA1 gene. (C) 1994 Academic Press, Inc.
引用
收藏
页码:310 / 312
页数:3
相关论文
共 50 条
  • [1] Extrapyramidal signs in autosomal dominant spinocerebellar ataxais (SCA1, SCA2, and SCA3)
    Pal, P. K.
    BS, Y.
    Puroshattam, M.
    Sinha, S.
    Jain, S.
    MOVEMENT DISORDERS, 2006, 21 : S334 - S334
  • [2] LINKAGE STUDIES IN SPINOCEREBELLAR ATAXIA (SCA1)
    ZOGHBI, HY
    POLLACK, MS
    FERRELL, RE
    DAIGER, SP
    LYONS, LA
    OBRIEN, WE
    BEAUDET, AL
    CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4): : 727 - 727
  • [3] Role of VEGF in spinocerebellar ataxia 1(SCA1)
    Cvetanovic, Marija
    Opal, Puneet
    JOURNAL OF NEUROIMMUNOLOGY, 2008, 203 (02) : 189 - 189
  • [4] POSITIONAL CLONING EFFORTS FOR SPINOCEREBELLAR ATAXIA (SCA1)
    KWIATKOWSKI, TJ
    MCCALL, AE
    CHINAULT, AC
    BEAUGER, AL
    ZOGHBI, HY
    AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 382 - 382
  • [5] THE MACHADO-JOSEPH DISEASE LOCUS IS DIFFERENT FROM THE SPINOCEREBELLAR ATAXIA LOCUS (SCA1)
    CARSON, WJ
    RADVANY, J
    FARRER, LA
    VINCENT, D
    ROSENBERG, RN
    MACLEOD, PM
    ROULEAU, GA
    GENOMICS, 1992, 13 (03) : 852 - 855
  • [6] Autosomal dominant cerebellar ataxia type I:: oculomotor abnormalities in families with SCA1, SCA2, and SCA3
    Bürk, K
    Fetter, M
    Abele, M
    Laccone, F
    Brice, A
    Dichgans, J
    Klockgether, T
    JOURNAL OF NEUROLOGY, 1999, 246 (09) : 789 - 797
  • [7] Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3
    K. Bürk
    M. Fetter
    M. Abele
    F. Laccone
    A. Brice
    J. Dichgans
    T. Klockgether
    Journal of Neurology, 1999, 246 : 789 - 797
  • [8] ANALYSIS OF SCA1 AND DRPLA MUTATIONS IN A LARGE POPULATION OF SPINOCEREBELLAR ATAXIA PATIENTS
    SILVEIRA, I
    LOPESCENDES, I
    KISH, S
    STEINER, CE
    PINTOJUNIOR, W
    MACIEL, JA
    BOTEZ, MI
    ARRUDA, W
    TIEVE, H
    JAIN, S
    SACK, G
    RADVANY, J
    ANDERMANN, E
    SEQUIROS, J
    ROULEAU, GA
    NEUROLOGY, 1995, 45 (04) : A422 - A422
  • [9] A 17TH-CENTURY FOUNDER GIVES RISE TO A LARGE NORTH-AMERICAN PEDIGREE OF AUTOSOMAL DOMINANT SPINOCEREBELLAR ATAXIA NOT LINKED TO THE SCA1 LOCUS ON CHROMOSOME-6
    LAZZARINI, A
    ZIMMERMAN, TR
    JOHNSON, WG
    DUVOISIN, RC
    NEUROLOGY, 1992, 42 (11) : 2118 - 2124
  • [10] DOMINANTLY INHERITED SPINOCEREBELLAR ATAXIA (SCA1) LINKAGE STUDIES
    SHRIMPTON, AE
    VIJAYALAXMI
    EVANS, HJ
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 1080 - 1080