LINKAGE MAPPING OF DOPA-RESPONSIVE DYSTONIA (DRD) TO CHROMOSOME 14Q

被引:155
作者
NYGAARD, TG
WILHELMSEN, KC
RISCH, NJ
BROWN, DL
TRUGMAN, JM
GILLIAM, TC
FAHN, S
WEEKS, DE
机构
[1] YALE UNIV,SCH MED,DEPT EPIDEMIOL & PUBL HLTH,NEW HAVEN,CT 06510
[2] YALE UNIV,SCH MED,DEPT GENET,NEW HAVEN,CT 06510
[3] UNIV PITTSBURGH,DEPT HUMAN GENET,PITTSBURGH,PA 15261
[4] UNIV VIRGINIA,HLTH SCI CTR,DEPT NEUROL,CHARLOTTESVILLE,VA 22908
[5] COLUMBIA PRESBYTERIAN MED CTR,DEPT PSYCHIAT,NEW YORK,NY 10032
[6] COLUMBIA PRESBYTERIAN MED CTR,DEPT GENET & DEV,NEW YORK,NY 10032
关键词
D O I
10.1038/ng1293-386
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Dopa-responsive dystonia (DRD) is an autosomal-dominant neurological disorder which appears to result from a genetically determined deficiency of striatal dopamine. Pathological evidence suggests that this may be due to the establishment of a reduced number of dopaminergic nerve terminals in the striatum, or to an excessive reduction (pruning) of these terminals in early development. We have mapped the DRD gene to chromosome 14 by linkage analysis in 3 families with a maximum 2-point lod score of 4.67 at 8.6 centiMorgans from D14S63; maximum multipoint lod scores >6 were obtained for the intervals D14S47-D14S52 and D14S52-D14S63. The flanking loci D14S47 and D14S63 define a region of about 22 cM as containing the DRD gene.
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页码:386 / 391
页数:6
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共 39 条
  • [1] SPONTANEOUS ORAL-FACIAL DYSKINESIA - NEUROPATHOLOGY OF A CASE
    ALTROCCHI, PH
    FORNO, LS
    [J]. NEUROLOGY, 1983, 33 (06) : 802 - 805
  • [2] BERNHEIMER H, 1973, J NEUROL SCI, V20, P415, DOI 10.1016/0022-510X(73)90175-5
  • [3] BOEHNKE M, 1991, AM J HUM GENET, V48, P22
  • [4] BRAVERMAN MS, 1985, COMPUT BIOMED RES, V8, P24
  • [5] IDIOPATHIC DYSTONIA AMONG ASHKENAZI JEWS - EVIDENCE FOR AUTOSOMAL DOMINANT INHERITANCE
    BRESSMAN, SB
    DELEON, D
    BRIN, MF
    RISCH, N
    BURKE, RE
    GREENE, PE
    SHALE, H
    FAHN, S
    [J]. ANNALS OF NEUROLOGY, 1989, 26 (05) : 612 - 620
  • [6] Cox Tara K., 1992, American Journal of Human Genetics, V51, pA33
  • [7] DAUSSET J, 1986, PRESSE MED, V15, P1801
  • [8] FAHN S, 1989, J NEUROL NEUROSUR PS, P96
  • [9] FAHN S, 1987, MOVEMENT DISORD, V2, P332
  • [10] DYSTONIA WITH MARKED DIURNAL-VARIATION ASSOCIATED WITH BIOPTERIN DEFICIENCY
    FINK, JK
    BARTON, N
    COHEN, W
    LOVENBERG, W
    BURNS, RS
    HALLETT, M
    [J]. NEUROLOGY, 1988, 38 (05) : 707 - 711