Hemophilia A: different phenotypes may be explained by multiple and variable effects of the causative mutation in the F8 gene

Benzer Materyaller

• The higher prevalence of missense mutations in hemophilia B compared to hemophilia A could be important in determining a milder clinical phenotype in patients with severe hemophilia B
  Yazar:: Melchiorre, Daniela, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Hemophilia A and B: molecular and clinical similarities and differences
  Yazar:: Castaman, Giancarlo, ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• Gene mutation may explain multiple-birth pregnancies
  Baskı/Yayın Bilgisi: (2001)
• Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations
  Yazar:: Boylan, Brian, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• Detection of F8 mutations in carriers and patients with severe hemophilia A. Identification of a novel mutation.
  Yazar:: Lucía López-Vásquez, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)