Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

Ítems similars

• Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
  per: Naz, Arshi, et al.
  Publicat: (2017)
• Mutation Spectrum and Genotype–Phenotype Analyses in a Pakistani Cohort With Hemophilia B
  per: Khan, Muhammad Tariq Masood, et al.
  Publicat: (2017)
• Diagnosis and phenotypic assessment of Pakistani Haemophilia B carriers
  per: Khan, Muhammad Tariq Masood, et al.
  Publicat: (2017)
• A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family
  per: Shahid, Saba, et al.
  Publicat: (2019)
• Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regions
  per: Naz, Arshi, et al.
  Publicat: (2017)