VWF c.2287_2289delinsTGT ;(p.R763C)

Variant ID: 12-6153610-CCT-ACA

NM_000552.3(VWF):c.2287_2289delinsTGT;(p.R763C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy.

Haematologica
Casonato, Alessandra A; Daidone, Viviana V; Barbon, Giovanni G; Pontara, Elena E; Di Pasquale, Irene I; Gallinaro, Lisa L; Marullo, Letizia L; Bertorelle, Giorgio G
Publication Date: 2013-01

Variant appearance in text: VWF: R763C
PubMed Link: 22875612
Variant Present in the following documents:
  • Main text
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