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

Liknande verk

• Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.
  av: Bunyan, D, et al.
  Publicerad: (2007)
• MLPA-based point mutation analysis of the FBN1 gene in Marfan syndrome patients.
  av: Bunyan, D, et al.
  Publicerad: (2004)
• MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India
  av: Sekar Deepha, et al.
  Publicerad: (2017-06-01)
• MLPA followed by target‐NGS to detect mutations in the dystrophin gene of Peruvian patients suspected of DMD/DMB
  av: María Luisa Guevara‐Fujita, et al.
  Publicerad: (2021-09-01)
• Identification of Exonic Copy Number Variations in Dystrophin Gene Using Mlpa / Identificarea Variaţiilor Numărului de Copii în Gena Distrofinei Folosind Metoda Mlpa
  av: Rusu Cristina, et al.
  Publicerad: (2014-12-01)