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Volumn 98, Issue 3, 1996, Pages 371-375

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 2P; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MALE; MARKER GENE; PRIORITY JOURNAL; SPASTIC PARAPLEGIA;

EID: 0029737834     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050223     Document Type: Article
Times cited : (31)

References (19)
  • 1
    • 0015945194 scopus 로고
    • Strümpell's familial spastic paraplegia: Genetics and neuropathology
    • Behan W, 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.1    Maia, M.2
  • 2
    • 0027263205 scopus 로고
    • Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch family
    • Bruyn RP, Deutekom J van, Frants RR, Padberg GW (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.1    Van Deutekom, J.2    Frants, R.R.3    Padberg, G.W.4
  • 7
    • 0020641096 scopus 로고
    • Classification of the hereditary ataxias and paraplegias
    • Harding AE (1983) Classification of the hereditary ataxias and paraplegias. Lancet I (8334) : 1151-1155
    • (1983) Lancet , vol.1 , Issue.8334 , pp. 1151-1155
    • Harding, A.E.1
  • 8
    • 0027759812 scopus 로고
    • Hereditary spastic paraplegias
    • Harding AE (1993) Hereditary spastic paraplegias. Semin Neurol 13 : 333-336
    • (1993) Semin Neurol , vol.13 , pp. 333-336
    • Harding, A.E.1
  • 9
    • 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, Recondo J de, Weissenbach J (1993) Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Nat Genet 5 : 163-167
    • (1993) Nat 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
  • 14
    • 0028146646 scopus 로고
    • Trinucleotide diseases on the rise
    • Mandel JL (1994) Trinucleotide diseases on the rise. Nat Genet 7: 453-455
    • (1994) Nat Genet , vol.7 , pp. 453-455
    • Mandel, J.L.1
  • 16
    • 0018837030 scopus 로고
    • Hereditary spastic paraplegia with neurogenic bladder disturbances and syndaetyly
    • Opjordsmoen S, Nyberg-Hansen R (1980) Hereditary spastic paraplegia with neurogenic bladder disturbances and syndaetyly. Acta Neurol Scand 61 : 35-41
    • (1980) Acta Neurol Scand , vol.61 , pp. 35-41
    • Opjordsmoen, S.1    Nyberg-Hansen, R.2
  • 18
    • 0028239867 scopus 로고
    • X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus
    • Saugier-Veber P, Munnich A, Bonneau D, Rozet JM, Le-Merrer M, Gil R, Boespflug-Tanguy O (1994) X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus. Nat Genet 6 : 257-262
    • (1994) Nat Genet , vol.6 , pp. 257-262
    • Saugier-Veber, P.1    Munnich, A.2    Bonneau, D.3    Rozet, J.M.4    Le-Merrer, M.5    Gil, R.6    Boespflug-Tanguy, O.7
  • 19
    • 0027434766 scopus 로고
    • Report and abstracts of the second international workshop on human chromosome 2 mapping
    • Spurr NK, Cox S, Naylor S (1993) Report and abstracts of the second international workshop on human chromosome 2 mapping. Cytogenet Cell Genet 64 : 69-92
    • (1993) Cytogenet Cell Genet , vol.64 , pp. 69-92
    • Spurr, N.K.1    Cox, S.2    Naylor, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.