메뉴 건너뛰기




Volumn 99, Issue 2, 1997, Pages 87-90

Familial spastic paraplegia: Evidence for a fourth locus

Author keywords

Familial spastic paraplegia; Genetic linkage; Heterogeneity

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 14Q; CHROMOSOME 15Q; CHROMOSOME 2P; CLINICAL ARTICLE; FAMILY STUDY; GENE LOCUS; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NETHERLANDS; SPASTIC PARAPLEGIA;

EID: 0031011298     PISSN: 03038467     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0303-8467(97)00602-1     Document Type: Article
Times cited : (5)

References (18)
  • 1
    • 0000047668 scopus 로고
    • Ph Scheltens. Hereditary spastic paraparesis (Strümpell-Lorrain)
    • P.J. Vinken, G.W. Bruyn and H.L. Klawans (Eds.), Amsterdam, Elsevier
    • Bruyn, R.P.M. (1992) Ph Scheltens. Hereditary spastic paraparesis (Strümpell-Lorrain). In: P.J. Vinken, G.W. Bruyn and H.L. Klawans (Eds.), Handbook of Clinical Neurology, Vol. 59, Amsterdam, Elsevier, pp. 301-318.
    • (1992) Handbook of Clinical Neurology , vol.59 , pp. 301-318
    • Bruyn, R.P.M.1
  • 3
    • 0019777963 scopus 로고
    • Hereditary 'pure' spastic paraplegia: A clinical and genetic study of 22 families
    • Harding, A.E. (1981) Hereditary 'pure' spastic paraplegia: a clinical and genetic study of 22 families. J. Neurol. Neurosurg. Psychiatry, 44: 871-883.
    • (1981) J. Neurol. Neurosurg. Psychiatry , vol.44 , pp. 871-883
    • Harding, A.E.1
  • 5
    • 0015945194 scopus 로고
    • Strümpell's familial spastic paraplegia: Genetics and neuropathology
    • Behan, W.M.H and Maia, M. (1974) Strümpell's familial spastic paraplegia: genetics and neuropathology. J. Neurol. Neurosurg. Psychiatry, 37: 8-20.
    • (1974) J. Neurol. Neurosurg. Psychiatry , vol.37 , pp. 8-20
    • Behan, W.M.H.1    Maia, M.2
  • 6
    • 0001432872 scopus 로고
    • Beiträge zur Pathologie des Rückenmarks
    • Strümpell, A. (1880) Beiträge zur Pathologie des Rückenmarks. Arch Psychiatr Nervenkr, 10: 676-717.
    • (1880) Arch Psychiatr Nervenkr , vol.10 , pp. 676-717
    • Strümpell, A.1
  • 7
    • 0027363223 scopus 로고
    • Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q
    • Hazan, J., Lamy, C., Melki, J., Munnich, A., de Recondo, J. and Weissenbach, J. (1993) Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Nature Genet., 5:163-167.
    • (1993) Nature Genet. , vol.5 , pp. 163-167
    • Hazan, J.1    Lamy, C.2    Melki, J.3    Munnich, A.4    De Recondo, J.5    Weissenbach, J.6
  • 10
    • 0027263205 scopus 로고
    • Hereditary spastic paraparesis: Clinical and genetic data from a large Dutch family
    • Bruyn, R.P.M., van Deutekom, J., Frants, R.R. and Padberg, G.W. (1993) Hereditary spastic paraparesis: clinical and genetic data from a large Dutch family. Clin. Neurol. Neurosurg., 95: 125-129.
    • (1993) Clin. Neurol. Neurosurg. , vol.95 , pp. 125-129
    • Bruyn, R.P.M.1    Van Deutekom, J.2    Frants, R.R.3    Padberg, G.W.4
  • 13
    • 0025124220 scopus 로고
    • A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease)
    • Scheltens, P., Bruyn, R.P.M, Hazenberg, G.J. (1990) A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease). Acta. Neurol. Scand., 82: 169-173.
    • (1990) Acta. Neurol. Scand. , vol.82 , pp. 169-173
    • Scheltens, P.1    Bruyn, R.P.M.2    Hazenberg, G.J.3
  • 16
    • 0023186341 scopus 로고
    • The autosomal dominant form of "pure" familial spastic paraplegia: Clinical findings and linkage analysis of a large pedigree
    • Boustany, R.M.N., Fleischnick, E., Alper, C.A., Marazita, M.L., Spence, M.A., Martin, J.B., Kolodny, E.H. (1987) The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree. Neurology, 37: 910-915.
    • (1987) Neurology , vol.37 , pp. 910-915
    • Boustany, R.M.N.1    Fleischnick, E.2    Alper, C.A.3    Marazita, M.L.4    Spence, M.A.5    Martin, J.B.6    Kolodny, E.H.7
  • 17
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detections of linkage and estimation of recombination
    • Lathrop, G.M., Lalouel, J.M., Julier, C. and Ott, J.(1985) Multilocus linkage analysis in humans: detections of linkage and estimation of recombination. Am. J. Hum. Genet., 37: 482-498.
    • (1985) Am. J. Hum. Genet. , vol.37 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.