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

Slični predmeti

• Simultaneous MLPA-based multiplex point mutation and deletion analysis of the dystrophin gene.
  od: Bunyan, D, i dr.
  Izdano: (2007)
• MLPA-based point mutation analysis of the FBN1 gene in Marfan syndrome patients.
  od: Bunyan, D, i dr.
  Izdano: (2004)
• MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India
  od: Sekar Deepha, i dr.
  Izdano: (2017-06-01)
• MLPA followed by target‐NGS to detect mutations in the dystrophin gene of Peruvian patients suspected of DMD/DMB
  od: María Luisa Guevara‐Fujita, i dr.
  Izdano: (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
  od: Rusu Cristina, i dr.
  Izdano: (2014-12-01)