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

Samankaltaisia teoksia

• Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.
  Tekijä: Bunyan, D, et al.
  Julkaistu: (2007)
• MLPA-based point mutation analysis of the FBN1 gene in Marfan syndrome patients.
  Tekijä: Bunyan, D, et al.
  Julkaistu: (2004)
• MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India
  Tekijä: Sekar Deepha, et al.
  Julkaistu: (2017-06-01)
• Identification of gross deletions in FBN1 gene by MLPA
  Tekijä: Hang Yang, et al.
  Julkaistu: (2018-10-01)
• Identification and characterization of dystrophin-locus-derived testis-specific protein: A testis-specific gene within the intronic region of the rat dystrophin gene
  Tekijä: Keitaro YAMANOUCHI, et al.
  Julkaistu: (2024-01-01)