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Volumn 9, Issue 8, 1999, Pages 552-554

Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies

Author keywords

Deletion pattern analysis; Duchenne Becker muscular dystrophy; Dystrophin gene

Indexed keywords

DYSTROPHIN;

EID: 0345580874     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(99)00044-9     Document Type: Article
Times cited : (11)

References (10)
  • 2
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    • Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies
    • Claustres M., Tuffery S., Chevron M.P., et al. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies. Hum Genet. 88:1991;179-184.
    • (1991) Hum Genet , vol.88 , pp. 179-184
    • Claustres, M.1    Tuffery, S.2    Chevron, M.P.3
  • 3
    • 0028940944 scopus 로고
    • Deletion patterns of Duchenne and Becker muscular dystrophies in Greece
    • Florentin L., Mavrou A., Kekou K., Metaxotou C. Deletion patterns of Duchenne and Becker muscular dystrophies in Greece. J Med Genet. 32:1995;48-51.
    • (1995) J Med Genet , vol.32 , pp. 48-51
    • Florentin, L.1    Mavrou, A.2    Kekou, K.3    Metaxotou, C.4
  • 4
    • 0028084292 scopus 로고
    • Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients
    • Shomrat R., Gluck E., Legum C., Shiloh Y. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients. Am J Med Genet. 49:1994;369-373.
    • (1994) Am J Med Genet , vol.49 , pp. 369-373
    • Shomrat, R.1    Gluck, E.2    Legum, C.3    Shiloh, Y.4
  • 5
    • 0029795153 scopus 로고    scopus 로고
    • Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intron
    • Todorova A., Bronzova J., Miorin M., Rosa M., Kremensky I., Danieli G.A. Mutation analysis in Duchenne and Becker muscular dystrophy patients from Bulgaria shows a peculiar distribution of breakpoints by intron. Am J Med Gen. 65:1996;40-43.
    • (1996) Am J Med Gen , vol.65 , pp. 40-43
    • Todorova, A.1    Bronzova, J.2    Miorin, M.3    Rosa, M.4    Kremensky, I.5    Danieli, G.A.6
  • 6
    • 0027198597 scopus 로고
    • Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR
    • Gökgöz N., Kuseyri F., Topaloglu H., Yüksel-Apak M., Kirdar B. Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR. Clin Genet. 43:1993;261-266.
    • (1993) Clin Genet , vol.43 , pp. 261-266
    • Gökgöz, N.1    Kuseyri, F.2    Topaloglu, H.3    Yüksel-Apak, M.4    Kirdar, B.5
  • 8
    • 0025244924 scopus 로고
    • Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
    • Beggs A.H., Koenig M., Boyce F.M., 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
  • 9
    • 0024245082 scopus 로고
    • Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
    • Chamberlain J.S., Gibbs R.A., Ranier J.E., Nguyen P.N., Caskey C.T. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucl Acids Res. 16:1988;11141-11156.
    • (1988) Nucl Acids Res , vol.16 , pp. 11141-11156
    • Chamberlain, J.S.1    Gibbs, R.A.2    Ranier, J.E.3    Nguyen, P.N.4    Caskey, C.T.5
  • 10
    • 0025774523 scopus 로고
    • A convenient multiplex PCR system for the detection of dystrophin gene deletions: A comparative analysis with cDNA hybridisation shows mistypings by both methods
    • Abbs S., Yau S.C., Clark S., Mathew C.G., Bobrow M. A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods. J Med Genet. 28:1991;304-311.
    • (1991) J Med Genet , vol.28 , pp. 304-311
    • Abbs, S.1    Yau, S.C.2    Clark, S.3    Mathew, C.G.4    Bobrow, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.