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Identification of a novel T-insertion polymorphism at the DMD locus

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Abstract

We have identified a novel T-insertion polymorphism located in the second intron of the dystrophin gene. This polymorphism should prove useful in linkage studies in Duchenne and Becker muscular dystrophy families in addition to the previously described markers.

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References

  • Beggs AH, Koenig M, Boyce F, Kunkel LM (1990) Detection of 8% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet 86:45–48

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  • Oudet C, Heilig R, Hanauer A, Mandel JL (1991) Nonradioactive assay for novel microsatellite polymorphism at the 5′ end of the dystrophin gene, and estimation of intragenic recombination. Am J Hum Genet 49:311–319

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Muntoni, F., Cau, M., Congiu, R. et al. Identification of a novel T-insertion polymorphism at the DMD locus. Hum Genet 92, 103 (1993). https://doi.org/10.1007/BF00216157

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  • DOI: https://doi.org/10.1007/BF00216157

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