VWF c.2281+4A>G

Variant ID: 12-6155885-T-C

NM_000552.3(VWF):c.2281+4A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Cellular and molecular basis of von Willebrand disease: studies on blood outgrowth endothelial cells.

Blood
Starke, Richard D RD; Paschalaki, Koralia E KE; Dyer, Clare E F CE; Harrison-Lavoie, Kimberly J KJ; Cutler, Jacqueline A JA; McKinnon, Thomas A J TA; Millar, Carolyn M CM; Cutler, Daniel F DF; Laffan, Mike A MA; Randi, Anna M AM
Publication Date: 2013-04-04

Variant appearance in text: VWF: 2281+4A>G
PubMed Link: 23355534
Variant Present in the following documents:
  • Main text
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