A new approach for the identification of common point mutations within the dystrophin gene using MLPA

Ítems similars

• Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.
  per: Bunyan, D, et al.
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• MLPA-based point mutation analysis of the FBN1 gene in Marfan syndrome patients.
  per: Bunyan, D, et al.
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• MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India
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• Identification of gross deletions in FBN1 gene by MLPA
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• Identification and characterization of dystrophin-locus-derived testis-specific protein: A testis-specific gene within the intronic region of the rat dystrophin gene
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