Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.

Lignende værker

• A new approach for the identification of common point mutations within the dystrophin gene using MLPA
  af: Skinner, A, et al.
  Udgivet: (2005)
• MLPA-based point mutation analysis of the FBN1 gene in Marfan syndrome patients.
  af: Bunyan, D, et al.
  Udgivet: (2004)
• MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India
  af: Sekar Deepha, et al.
  Udgivet: (2017-06-01)
• Characterisation of beta globin gene cluster deletions using multiplex-Gap-PCR and Multiplex Ligation-dependent Probe Amplification (MLPA)
  af: Redzuwan, Yasmin Mohamad
  Udgivet: (2018)
• Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion
  af: Wittaya Jomoui, et al.
  Udgivet: (2023-06-01)