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Volumn 42, Issue 1, 1997, Pages 111-114

Sporadic focal dystonia in Northwest Germany: Molecular basis on chromosome 18p

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 18P; CHROMOSOME MAP; DNA DETERMINATION; DYSTONIA; GERMANY; HUMAN; PENETRANCE; PRIORITY JOURNAL; TORSION DYSTONIA;

EID: 0030875011     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420117     Document Type: Article
Times cited : (60)

References (18)
  • 1
    • 0023675531 scopus 로고
    • Concept and classification of dystonia
    • Fahn S. Concept and classification of dystonia. Adv Neurol 1988;50:1-8
    • (1988) Adv Neurol , vol.50 , pp. 1-8
    • Fahn, S.1
  • 2
    • 0000613043 scopus 로고
    • Classification and investigation of dystonia
    • Marsden CD, Fahn S, eds. London: Butterworths
    • Fahn S, Marsden CD, Calne DB. Classification and investigation of dystonia. In: Marsden CD, Fahn S, eds. Movement disorders 2. London: Butterworths, 1987:332-358
    • (1987) Movement Disorders 2 , pp. 332-358
    • Fahn, S.1    Marsden, C.D.2    Calne, D.B.3
  • 3
    • 0002997334 scopus 로고
    • Dystonias
    • Jankovic J, Hallet M, eds. New York: Marcel Dekker
    • Fahn S. Dystonias. In: Jankovic J, Hallet M, eds. Therapy with botulinum toxin. New York: Marcel Dekker, 1994:173-189
    • (1994) Therapy with Botulinum Toxin , pp. 173-189
    • Fahn, S.1
  • 4
    • 0023757658 scopus 로고
    • Epidemiology of dystonia in Rochester, Minnesota
    • Nutt JG, Muenter MD, Melton LJ, et al. Epidemiology of dystonia in Rochester, Minnesota. Adv Neurol 1988;50:361-365
    • (1988) Adv Neurol , vol.50 , pp. 361-365
    • Nutt, J.G.1    Muenter, M.D.2    Melton, L.J.3
  • 5
    • 0026099811 scopus 로고
    • A genetic study of idiopathic focal dystonia
    • Waddy HM, Fletcher A, Harding AE, et al. A genetic study of idiopathic focal dystonia. Ann Neurol 1991;29:320-324
    • (1991) Ann Neurol , vol.29 , pp. 320-324
    • Waddy, H.M.1    Fletcher, A.2    Harding, A.E.3
  • 6
    • 0029052823 scopus 로고
    • A genetic study of idiopathic focal dystonias
    • Stojanovic M, Cvetkovic D, Kostic VS. A genetic study of idiopathic focal dystonias. J Neurol 1995;242:508-511
    • (1995) J Neurol , vol.242 , pp. 508-511
    • Stojanovic, M.1    Cvetkovic, D.2    Kostic, V.S.3
  • 7
    • 0024657745 scopus 로고
    • Human gene for torsion dystonia is located on chromosome 9q32-q34
    • Ozelius L, Kramer PL, Moskowitz CB, et al. Human gene for torsion dystonia is 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
  • 8
    • 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
  • 9
    • 0026071238 scopus 로고
    • Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome
    • Wilhelmsem KC, Weeks DE, Nygaard TG, et al. Genetic mapping of "Lubag" (X-linked dystonia-parkinsonism) in a Filipino kindred to the pericentromeric region of the X chromosome. Ann Neurol 1991;29:124-131
    • (1991) Ann Neurol , vol.29 , pp. 124-131
    • Wilhelmsem, K.C.1    Weeks, D.E.2    Nygaard, T.G.3
  • 10
    • 0028106815 scopus 로고
    • DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DTY3)
    • Müller U, Haberhausen G, Wagner T, et al. DXS106 and DXS559 flank the X-linked dystonia-parkinsonism syndrome locus (DTY3). Genomics 1994;23:114-117
    • (1994) Genomics , vol.23 , pp. 114-117
    • Müller, U.1    Haberhausen, G.2    Wagner, T.3
  • 11
    • 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. Nature Genet 1994;8:236-242
    • (1994) Nature Genet , vol.8 , pp. 236-242
    • Ichinose, H.1    Ohye, T.2    Takahashi, E.3
  • 12
    • 0029049876 scopus 로고
    • Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene
    • Knappskog PM, Flatmark T, Mallet J, et al. Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene. Hum Mol Genet 1995;4:1209-1212
    • (1995) Hum Mol Genet , vol.4 , pp. 1209-1212
    • Knappskog, P.M.1    Flatmark, T.2    Mallet, J.3
  • 13
    • 0029896267 scopus 로고    scopus 로고
    • A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q
    • Fouad GT, Servidei S, Durcan S, et al. A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am J Hum Genet 1996;59:135-139
    • (1996) Am J Hum Genet , vol.59 , pp. 135-139
    • Fouad, G.T.1    Servidei, S.2    Durcan, S.3
  • 14
    • 0029937084 scopus 로고    scopus 로고
    • Paroxysmal dystonic choreoathetosis: Tight linkage to chromosome 2q
    • Fink JK, Rainier S, Wilkowski J, et al. Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q. Am J Hum Genet 1996;59:140-145
    • (1996) Am J Hum Genet , vol.59 , pp. 140-145
    • Fink, J.K.1    Rainier, S.2    Wilkowski, J.3
  • 15
    • 0030027095 scopus 로고    scopus 로고
    • A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197
    • Auburger G, Ratzlaff T, Lunkes A, et al. A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197. Genomics 1996;31:90-94
    • (1996) Genomics , vol.31 , pp. 90-94
    • Auburger, G.1    Ratzlaff, T.2    Lunkes, A.3
  • 16
    • 0029798561 scopus 로고    scopus 로고
    • Idiopathic torsion dystonia: Assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant 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 dominant 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
  • 17
    • 0026581762 scopus 로고
    • Strong allelic association between the torsion dystonia gene (DYT1) and loci on chromosome 9q34 in Ashkenazi Jews
    • Ozelius LJ, Kramer PL, de Leon D, et al. Strong allelic association between the torsion dystonia gene (DYT1) and loci on chromosome 9q34 in Ashkenazi Jews. Am J Hum Genet 1992; 50:619-628
    • (1992) Am J Hum Genet , vol.50 , pp. 619-628
    • Ozelius, L.J.1    Kramer, P.L.2    De Leon, D.3
  • 18
    • 0024582679 scopus 로고
    • Linkage disequilibrium, cystic fibrosis and genetic counselling
    • Beaudet AL, Feldman GL, Fernbach SD, et al. Linkage disequilibrium, cystic fibrosis and genetic counselling. Am J Hum Genet 1989;44:319-326
    • (1989) Am J Hum Genet , vol.44 , pp. 319-326
    • Beaudet, A.L.1    Feldman, G.L.2    Fernbach, S.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.