VWF c.5035A>G ;(p.T1679A)

Variant ID: 12-6127549-T-C

NM_000552.3(VWF):c.5035A>G;(p.T1679A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Von Willebrand Factor Abnormalities Studied in the Mouse Model: What We Learned about VWF Functions.

Mediterranean Journal Of Hematology And Infectious Diseases
Casari, Caterina C; Lenting, Peter J PJ; Christophe, Olivier D OD; Denis, Cécile V CV
Publication Date: 2013

Variant appearance in text: VWF: T1679A
PubMed Link: 23936618
Variant Present in the following documents:
  • Main text
  • mjhid-5-1-e2013047.pdf
View BVdb publication page



In vivo analysis of the role of O-glycosylations of von Willebrand factor.

Plos One
Badirou, Idinath I; Kurdi, Mohamad M; Legendre, Paulette P; Rayes, Julie J; Bryckaert, Marijke M; Casari, Caterina C; Lenting, Peter J PJ; Christophe, Olivier D OD; Denis, Cecile V CV
Publication Date: 2012

Variant appearance in text: VWF: T1679A
PubMed Link: 22616016
Variant Present in the following documents:
  • pone.0037508.pdf
View BVdb publication page