Molecular pathogenesis of a novel Met394Thr variant causing hemophilia B

Míreanna comhchosúla

• Molecular pathogenesis of a novel Met394Thr variant causing hemophilia B
  de réir: Linna Lu, et al.
  Foilsithe / Cruthaithe: (2023-05-01)
• A novel dinucleotide variant at 5′ splice sites in the F8 gene causes exon 19 skipping in a Chinese family with hemophilia A
  de réir: Xunzhao Zhou, et al.
  Foilsithe / Cruthaithe: (2025-10-01)
• Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants
  de réir: Fucheng Li, et al.
  Foilsithe / Cruthaithe: (2023-12-01)
• Molecular mechanisms and therapeutic strategies for the recurrent F9 (c.520 + 13 A > G) variant in hemophilia B
  de réir: Huayang Zhang, et al.
  Foilsithe / Cruthaithe: (2026-01-01)
• Comprehensive Screening of Genetic Variants in the Coding Region of <i>F8</i> in Severe Hemophilia A Reveals a Relationship with Disease Severity in a Colombian Cohort
  de réir: Samuel Sarmiento Doncel, et al.
  Foilsithe / Cruthaithe: (2024-08-01)