VWF c.5053+1G>T

Variant ID: 12-6127530-C-A

NM_000552.3(VWF):c.5053+1G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort.

Thrombosis And Haemostasis
Hampshire, Daniel J DJ; Abuzenadah, Adel M AM; Cartwright, Ashley A; Al-Shammari, Nawal S NS; Coyle, Rachael E RE; Eckert, Michaela M; Al-Buhairan, Ahlam M AM; Messenger, Sarah L SL; Budde, Ulrich U; Gürsel, Türkiz T; Ingerslev, Jørgen J; Peake, Ian R IR; Goodeve, Anne C AC
Publication Date: 2013-08

Variant appearance in text: VWF: 5053+1G>T
PubMed Link: 23702511
Variant Present in the following documents:
  • Main text
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