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Clinical Genetics
Volumn 66, Issue 3, 2004, Pages 247-250
A shared chromosome-21 haplotype among amyotrophic lateral sclerosis families with the A4V SOD1 mutation [2]
Author keywords

[No Author keywords available]
Indexed keywords

ALANINE; COPPER ZINC SUPEROXIDE DISMUTASE; MICROSATELLITE DNA; VALINE;
EID: 4544327832     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2004.00298.x     Document Type: Letter
Times cited : (13)
References (10)
  • 1
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    • Tandan, R.1    Bradley, W.G.2
  • 2
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    • Amyotrophic lateral sclerosis. Part 2. Etiopathogenesis
    • Tandan R, Bradley WG. Amyotrophic lateral sclerosis. Part 2. Etiopathogenesis. Ann Neurol 1985: 18: 419-431.
    • (1985) Ann. Neurol. , vol.18 , pp. 419-431
    • Tandan, R.1    Bradley, W.G.2
  • 3
    • 12044249765 scopus 로고
    • Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity
    • Siddique T, Figlewicz DA, Pericak-Vance MA et al. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. N Engl J Med 1991: 324: 1381-1384.
    • (1991) N. Engl. J. Med. , vol.324 , pp. 1381-1384
    • Siddique, T.1    Figlewicz, D.A.2    Pericak-Vance, M.A.3
  • 4
    • 0027401203 scopus 로고
    • Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
    • Rosen DR, Siddique T, Patterson D et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993: 362: 59-62.
    • (1993) Nature , vol.362 , pp. 59-62
    • Rosen, D.R.1    Siddique, T.2    Patterson, D.3
  • 5
    • 0034209203 scopus 로고    scopus 로고
    • New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes
    • Kato S, Takikawa M, Nakashima K et al. New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes. ALS 2001: 1: 163-184.
    • (2001) ALS , vol.1 , pp. 163-184
    • Kato, S.1    Takikawa, M.2    Nakashima, K.3
  • 6
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    • A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis
    • Rosen DR, Bowling AC, Patterson D et al. A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis. Hum Mol Genet 1994: 3: 981-987.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 981-987
    • Rosen, D.R.1    Bowling, A.C.2    Patterson, D.3
  • 7
    • 0026526450 scopus 로고
    • Dinucleotide repeat (GT)n markers on chromosome 21
    • Warren AC, McInnis MG, Blaschak J et al. Dinucleotide repeat (GT)n markers on chromosome 21. Genomics 1992: 14: 818-819.
    • (1992) Genomics , vol.14 , pp. 818-819
    • Warren, A.C.1    McInnis, M.G.2    Blaschak, J.3
  • 8
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    • Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1
    • Rosen DR, Sapp PC, O-Regan J et al. Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1. Hum Mol Genet 1992: 1: 547.
    • (1992) Hum. Mol. Genet. , vol.1 , pp. 547
    • Rosen, D.R.1    Sapp, P.C.2    O-Regan, J.3
  • 9
    • 0028324543 scopus 로고
    • Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers
    • Rosen DR, Sapp P, O'Regan J et al. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers. Am J Med Genet 1994: 51: 61-69.
    • (1994) Am. J. Med. Genet. , vol.51 , pp. 61-69
    • Rosen, D.R.1    Sapp, P.2    O'Regan, J.3
  • 10
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    • The NCBI handbook [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information; 2002 October, January 14, release. Retrieved from
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    • (2003)

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.