메뉴 건너뛰기




Volumn 42, Issue 4, 1997, Pages 670-673

Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 8; ETHNIC GROUP; FEMALE; GENETIC LINKAGE; HAPLOTYPE; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; TORSION DYSTONIA;

EID: 0030868892     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420421     Document Type: Article
Times cited : (169)

References (27)
  • 1
    • 0024657745 scopus 로고
    • Human gene for torsion dystonia located on chromosome 9q32-q34
    • Ozelius L, Kramer PL, Moskowitz CB, et al. Human gene for torsion dystonia located on chromosome 9q32-q34. Neuron 1989;2:1427-1434
    • (1989) Neuron , vol.2 , pp. 1427-1434
    • Ozelius, L.1    Kramer, P.L.2    Moskowitz, C.B.3
  • 2
    • 0025238901 scopus 로고
    • Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
    • Kramer PL, de Leon D, Ozelius L, et al. Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34. Ann Neurol 1990;27:114-120
    • (1990) Ann Neurol , vol.27 , pp. 114-120
    • Kramer, P.L.1    De Leon, D.2    Ozelius, L.3
  • 3
    • 0028819262 scopus 로고
    • Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population
    • Risch N, deLeon D, Ozelius L, et al. Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. Nat Genet 1995;9:152-159
    • (1995) Nat Genet , vol.9 , pp. 152-159
    • Risch, N.1    DeLeon, D.2    Ozelius, L.3
  • 4
    • 0028097164 scopus 로고
    • Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia
    • Bressman SB, Hunt AL, Heiman GA, et al. Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia. Mov Disord 1994;9:626-632
    • (1994) Mov Disord , vol.9 , pp. 626-632
    • Bressman, S.B.1    Hunt, A.L.2    Heiman, G.A.3
  • 5
    • 0028344689 scopus 로고
    • A study of idiopathic torsion dystonia in a non-Jewish family - Evidence for genetic heterogeneity
    • Bressman SB, Heiman GA, Nygaard TG, et al. A study of idiopathic torsion dystonia in a non-Jewish family - evidence for genetic heterogeneity. Neurology 1994;44:283-287
    • (1994) Neurology , vol.44 , pp. 283-287
    • Bressman, S.B.1    Heiman, G.A.2    Nygaard, T.G.3
  • 6
    • 0029133628 scopus 로고
    • Adult onset idiopathic torsion dystonia is excluded from the DYT1 region (9q34) in a Swedish family
    • Holmgren G, Ozelius L, Forsgren L, et al. Adult onset idiopathic torsion dystonia is excluded from the DYT1 region (9q34) in a Swedish family. J Neurol Neurosurg Psychiatry 1995;59:178-181
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 178-181
    • Holmgren, G.1    Ozelius, L.2    Forsgren, L.3
  • 7
    • 10244255192 scopus 로고    scopus 로고
    • Exclusion of the DYT1 locus in familial torticollis
    • Bressman SB, Warner TT, Almasy L, et al. Exclusion of the DYT1 locus in familial torticollis. Ann Neurol 1996;40:681-684
    • (1996) Ann Neurol , vol.40 , pp. 681-684
    • Bressman, S.B.1    Warner, T.T.2    Almasy, L.3
  • 8
    • 0029798561 scopus 로고    scopus 로고
    • Idiopathic torsion dystonia: Assignment of a gene to chromosome 18p in a German family with adult onset, autosomal inheritance and purely focal distribution
    • Leube B, Rudnicki D, Ratzlaff T, et al. Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal inheritance and purely focal distribution. Hum Mol Genet 1996;5:1673-1677
    • (1996) Hum Mol Genet , vol.5 , pp. 1673-1677
    • Leube, B.1    Rudnicki, D.2    Ratzlaff, T.3
  • 9
    • 0024457283 scopus 로고
    • Idiopathic dystonia among Ashkenazi Jews: Evidence for autosomal dominant inheritance
    • Bressman SB, de Leon D, Brin MF, et al. Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Ann Neurol 1989;26:612-620
    • (1989) Ann Neurol , vol.26 , pp. 612-620
    • Bressman, S.B.1    De Leon, D.2    Brin, M.F.3
  • 10
    • 0023933932 scopus 로고
    • Efficient computations in multilocus linkage analysis
    • Lathrop GM, Lalouel JM. Efficient computations in multilocus linkage analysis. Am J Hum Genet 1988;42:498-505
    • (1988) Am J Hum Genet , vol.42 , pp. 498-505
    • Lathrop, G.M.1    Lalouel, J.M.2
  • 11
    • 0028790963 scopus 로고
    • The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
    • O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 1995;11:402-408
    • (1995) Nat Genet , vol.11 , pp. 402-408
    • O'Connell, J.R.1    Weeks, D.E.2
  • 12
    • 0000801438 scopus 로고
    • SLINK: A general simulation program for linkage analysis
    • Abstract
    • Weeks DE, Ott J, Lathrop GM. SLINK: a general simulation program for linkage analysis. Am J Hum Genet 1990;47:A204 (Abstract)
    • (1990) Am J Hum Genet , vol.47
    • Weeks, D.E.1    Ott, J.2    Lathrop, G.M.3
  • 14
    • 0029135425 scopus 로고
    • Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1
    • Haberhausen G, Schmitt I, Kohler A, et al. Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1. Am J Hum Genet 1995;57:644-650
    • (1995) Am J Hum Genet , vol.57 , pp. 644-650
    • Haberhausen, G.1    Schmitt, I.2    Kohler, A.3
  • 15
    • 0027401233 scopus 로고
    • Evidence for locus heterogeneity in autosomal dominant torsion dystonia
    • Ahmad F, Davis MB, Waddy HM, et al. Evidence for locus heterogeneity in autosomal dominant torsion dystonia. Genomics 1993;15:9-12
    • (1993) Genomics , vol.15 , pp. 9-12
    • Ahmad, F.1    Davis, M.B.2    Waddy, H.M.3
  • 16
    • 0028151448 scopus 로고
    • Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene
    • Ichinose H, Ohye T, Takahashi E, et al. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nat Genet 1994;8:236-242
    • (1994) Nat Genet , vol.8 , pp. 236-242
    • Ichinose, H.1    Ohye, T.2    Takahashi, E.3
  • 17
    • 0029182388 scopus 로고
    • Report and abstracts of the second international workshop on human chromosome 8 mapping 1994
    • Spurr NK, Blanton S, Bookstein R, et al. Report and abstracts of the second international workshop on human chromosome 8 mapping 1994. Cytogenet Cell Genet 1995;68:147-164
    • (1995) Cytogenet Cell Genet , vol.68 , pp. 147-164
    • Spurr, N.K.1    Blanton, S.2    Bookstein, R.3
  • 18
    • 0025349214 scopus 로고
    • Molecular cloning and expression of the cDNA for a novel alpha 1-adrenergic receptor subtype
    • Schwinn DA, Lomasney JW, Lorenz W, et al. Molecular cloning and expression of the cDNA for a novel alpha 1-adrenergic receptor subtype. J Biol Chem 1990;265:8183-8189
    • (1990) J Biol Chem , vol.265 , pp. 8183-8189
    • Schwinn, D.A.1    Lomasney, J.W.2    Lorenz, W.3
  • 19
    • 0025940707 scopus 로고
    • Molecular characterization of the mouse beta 3-adrenergic receptor: Relationship with the atypical receptor of adipocytes
    • Nahmias C, Blin N, Elalouf JM, et al. Molecular characterization of the mouse beta 3-adrenergic receptor: relationship with the atypical receptor of adipocytes. EMBO J 1991;10:3721-3727
    • (1991) EMBO J , vol.10 , pp. 3721-3727
    • Nahmias, C.1    Blin, N.2    Elalouf, J.M.3
  • 20
    • 0022475347 scopus 로고
    • Brain neurotransmitters in dystonia musculorum deformans
    • Hornykiewicz O, Kish SJ, Becker LE, et al. Brain neurotransmitters in dystonia musculorum deformans. N Engl J Med 1986;315:347-353
    • (1986) N Engl J Med , vol.315 , pp. 347-353
    • Hornykiewicz, O.1    Kish, S.J.2    Becker, L.E.3
  • 21
    • 0023140022 scopus 로고
    • Brain neurotransmitters in dystonia
    • Jankovic J, Svendsen CN. Brain neurotransmitters in dystonia. N Engl J Med 1987;316:278-279
    • (1987) N Engl J Med , vol.316 , pp. 278-279
    • Jankovic, J.1    Svendsen, C.N.2
  • 22
    • 0027988344 scopus 로고
    • Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutation
    • Bressman SB, deLeon D, Kramer PL, et al. Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation. Ann Neurol 1994;36:771-777
    • (1994) Ann Neurol , vol.36 , pp. 771-777
    • Bressman, S.B.1    DeLeon, D.2    Kramer, P.L.3
  • 23
    • 0027930349 scopus 로고
    • The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews
    • Kramer PL, Heiman GA, Gasser T, et al. The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews. Am J Hum Genet 1994;55:468-475
    • (1994) Am J Hum Genet , vol.55 , pp. 468-475
    • Kramer, P.L.1    Heiman, G.A.2    Gasser, T.3
  • 24
    • 0028950638 scopus 로고
    • Spread of symptoms in idiopathic torsion dystonia
    • Greene P, Kang UJ, Fahn S. Spread of symptoms in idiopathic torsion dystonia. Mov Disord 1995;10:143-152
    • (1995) Mov Disord , vol.10 , pp. 143-152
    • Greene, P.1    Kang, U.J.2    Fahn, S.3
  • 25
    • 23544445193 scopus 로고    scopus 로고
    • A large Italian family affected by idiopathic torsion dystonia with complete penetrance, not linked to DYT1
    • Abstract
    • Bentivoglio AR, Albanese A, DelGrosso N, et al. A large Italian family affected by idiopathic torsion dystonia with complete penetrance, not linked to DYT1. Neurology 1996;46(suppl): A385 (Abstract)
    • (1996) Neurology , vol.46 , Issue.SUPPL.
    • Bentivoglio, A.R.1    Albanese, A.2    DelGrosso, N.3
  • 27
    • 0027482096 scopus 로고
    • Genetic contribution to idiopathic adult-onset blepharospasm and cranial-cervical dystonia
    • Defazio G, Livrea P, Guanti G, et al. Genetic contribution to idiopathic adult-onset blepharospasm and cranial-cervical dystonia. Eur Neurol 1993;33:345-350
    • (1993) Eur Neurol , vol.33 , pp. 345-350
    • Defazio, G.1    Livrea, P.2    Guanti, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.