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Volumn 252, Issue 1, 2007, Pages 1-3

Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal

Author keywords

Becker muscular dystrophy; Duchenne muscular dystrophy; Dystrophin deletions; Genetics; Molecular biology; Polymerase chain reaction

Indexed keywords

DYSTROPHIN;

EID: 33845440933     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jns.2006.06.025     Document Type: Article
Times cited : (11)

References (11)
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  • 2
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    • Koenig, M.1    Hoffman, E.P.2    Bertelson, C.J.3    Monaco, A.P.4    Feener, C.5    Kunkel, L.M.6
  • 3
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    • Topography of the Duchenne muscular dystrophy (DMD) gene : FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications
    • Den Dunnen J.T., Grootscholten P.M., Bakker E., Blonden L.A., Ginjaar H.B., Waapenaar M.C., et al. Topography of the Duchenne muscular dystrophy (DMD) gene : FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications. Am J Hum Genet 45 (1989) 835-847
    • (1989) Am J Hum Genet , vol.45 , pp. 835-847
    • Den Dunnen, J.T.1    Grootscholten, P.M.2    Bakker, E.3    Blonden, L.A.4    Ginjaar, H.B.5    Waapenaar, M.C.6
  • 4
    • 0025244924 scopus 로고
    • Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
    • Beggs A.H., Koenig M., Boyce F.M., and Kunkel L.M. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet 86 (1990) 45-48
    • (1990) Hum Genet , vol.86 , pp. 45-48
    • Beggs, A.H.1    Koenig, M.2    Boyce, F.M.3    Kunkel, L.M.4
  • 5
    • 0027936884 scopus 로고
    • Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected
    • Ballo R., Viljoen D., and Beighton P. Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected. SAMJ S Afr Med J 84 (1994) 494-497
    • (1994) SAMJ S Afr Med J , vol.84 , pp. 494-497
    • Ballo, R.1    Viljoen, D.2    Beighton, P.3
  • 6
    • 0027793431 scopus 로고
    • Genetic analysis of 60 Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) patients using dystrophin cDNA
    • Zhang J. Genetic analysis of 60 Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) patients using dystrophin cDNA. Zhongguo Yi Xue Ke Xue Yuan Xue Bao 15 6 (Dec 1993) 399-404
    • (1993) Zhongguo Yi Xue Ke Xue Yuan Xue Bao , vol.15 , Issue.6 , pp. 399-404
    • Zhang, J.1
  • 7
    • 0026062480 scopus 로고
    • DNA Polymorphysisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese
    • Soong B.W., Tsai T.F., Su C.H., Kao K.P., Hsiao K.J., and Su T.S. DNA Polymorphysisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese. Am J Med Genet 38 4 (Mar 15 1991) 593-600
    • (1991) Am J Med Genet , vol.38 , Issue.4 , pp. 593-600
    • Soong, B.W.1    Tsai, T.F.2    Su, C.H.3    Kao, K.P.4    Hsiao, K.J.5    Su, T.S.6
  • 8
    • 0027295665 scopus 로고
    • Deletion detection for diagnosis of Duchenne muscular dystrophy in the Japanese population - comparison between the polymerase chain reaction and the Southern Blot analysis
    • Katayama S., Takeshita S., Yauo T., Ubagai T., Qiu X.J., Katagiri Y., et al. Deletion detection for diagnosis of Duchenne muscular dystrophy in the Japanese population - comparison between the polymerase chain reaction and the Southern Blot analysis. Jpn J Hum Genet 38 2 (June 1993) 177-184
    • (1993) Jpn J Hum Genet , vol.38 , Issue.2 , pp. 177-184
    • Katayama, S.1    Takeshita, S.2    Yauo, T.3    Ubagai, T.4    Qiu, X.J.5    Katagiri, Y.6
  • 9
    • 0027275621 scopus 로고
    • Detection of partial deletion and partial duplication of the dystrophin gene in Japanese patients with Duchenne or Becker muscular dystrophy
    • Hiyama K., Kodaira M., Satoh C., Karakawa T., Kameo H., and Yamakido M. Detection of partial deletion and partial duplication of the dystrophin gene in Japanese patients with Duchenne or Becker muscular dystrophy. Jpn J Hum Genet 38 2 (Jun 1993) 169-176
    • (1993) Jpn J Hum Genet , vol.38 , Issue.2 , pp. 169-176
    • Hiyama, K.1    Kodaira, M.2    Satoh, C.3    Karakawa, T.4    Kameo, H.5    Yamakido, M.6
  • 10
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    • Amplification of Ten deletion-rich exons of the dystrophin gene by polymerase chain reaction shows deletions in 36 of 90 Japanese families with Duchenne muscular dystrophy
    • Kitoh Y., Matsuo M., Nishio H., Takumi T., Nakajima T., Masumura T., et al. Amplification of Ten deletion-rich exons of the dystrophin gene by polymerase chain reaction shows deletions in 36 of 90 Japanese families with Duchenne muscular dystrophy. Am J Med Genet 42 4 (Feb 15 1992) 453-457
    • (1992) Am J Med Genet , vol.42 , Issue.4 , pp. 453-457
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.