VWF c.1657dup ;(p.W553Lfs*97)

Variant ID: 12-6167086-C-CA

NM_000552.3(VWF):c.1657dup;(p.W553Lfs*97)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Abnormal angiogenesis in blood outgrowth endothelial cells derived from von Willebrand disease patients.

Blood Coagulation & Fibrinolysis : An International Journal In Haemostasis And Thrombosis
Selvam, Soundarya N SN; Casey, Lara J LJ; Bowman, Mackenzie L ML; Hawke, Lindsey G LG; Longmore, Avery J AJ; Mewburn, Jeffrey J; Ormiston, Mark L ML; Archer, Stephen L SL; Maurice, Donald H DH; James, Paula P
Publication Date: 2017-10

Variant appearance in text: VWF: 1657dupT; Trp553Leufs
PubMed Link: 28362648
Variant Present in the following documents:
  • Main text
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