TYROSINE-HYDROXYLASE POLYMORPHISM IN FAMILIAL AND SPORADIC PARKINSONS-DISEASE

被引:36
作者
PLANTEBORDENEUVE, V
DAVIS, MB
MARAGANORE, DM
MARSDEN, CD
HARDING, AE
机构
[1] UNIV LONDON,INST NEUROL,DEPT CLIN NEUROL,NEUROGENET SECT,LONDON WC1N 3BG,ENGLAND
[2] UNIV LONDON,INST NEUROL,DEPT CLIN NEUROL,MOVEMENT DISORDERS SECT,LONDON WC1N 3BG,ENGLAND
关键词
TYROSINE HYDROXYLASE; PARKINSONS DISEASE; LINKAGE ANALYSIS;
D O I
10.1002/mds.870090312
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tyrosine hydroxylase (TH) is a theoretical candidate gene determining susceptibility to Parkinson's disease (PD), and an association between one allele of a polymorphism at the TH locus and sporadic PD has been reported. We investigated TH polymorphism in 44 patients with sporadic PD, 48 patients with familial PD and 89 of their unaffected relatives, and 50 control subjects. No evidence of allelic association was detected in either familial or sporadic PD, and linkage analysis excluded the TH locus, or a closely linked gene, as a major determinant of familial PD.
引用
收藏
页码:337 / 339
页数:3
相关论文
共 17 条
  • [1] MUTANT DEBRISOQUINE HYDROXYLATION GENES IN PARKINSONS-DISEASE
    ARMSTRONG, M
    DALY, AK
    CHOLERTON, S
    BATEMAN, DN
    IDLE, JR
    [J]. LANCET, 1992, 339 (8800) : 1017 - 1018
  • [2] BISHOP DT, 1990, AM J HUM GENET, V46, P254
  • [3] PARKINSONS-DISEASE IN TWINS STUDIED WITH F-18 DOPA AND POSITRON EMISSION TOMOGRAPHY
    BURN, DJ
    MARK, MH
    PLAYFORD, ED
    MARAGANORE, DM
    ZIMMERMAN, TR
    DUVOISIN, RC
    HARDING, AE
    MARSDEN, CD
    BROOKS, DJ
    [J]. NEUROLOGY, 1992, 42 (10) : 1894 - 1900
  • [4] A PARKINSONIAN KINDRED
    DEGL'INNOCENTI, F
    MAURELLO, MT
    MARINI, P
    [J]. ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1989, 10 (03): : 307 - 310
  • [5] A LARGE KINDRED WITH AUTOSOMAL DOMINANT PARKINSONS-DISEASE
    GOLBE, LI
    DIIORIO, G
    BONAVITA, V
    MILLER, DC
    DUVOISIN, RC
    [J]. ANNALS OF NEUROLOGY, 1990, 27 (03) : 276 - 282
  • [6] H/CEPH Collaborative Mapping Group, 1992, SCIENCE, V258, P67
  • [7] A MAEIII POLYMORPHISM WITHIN INTRON-A OF THE INSULIN (INS) GENE DETECTABLE BY PCR
    HOBAN, PR
    KELSEY, AM
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (18) : 5091 - 5091
  • [8] TWIN STUDIES AND THE GENETICS OF PARKINSONS-DISEASE - A REAPPRAISAL
    JOHNSON, WG
    HODGE, SE
    DUVOISIN, R
    [J]. MOVEMENT DISORDERS, 1990, 5 (03) : 187 - 194
  • [9] KURTH JH, 1992, MOVEMENT DISORD, V7, P290
  • [10] STRATEGIES FOR MULTILOCUS LINKAGE ANALYSIS IN HUMANS
    LATHROP, GM
    LALOUEL, JM
    JULIER, C
    OTT, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (11): : 3443 - 3446