F7 c.226-672A>G

Variant ID: 13-113767394-A-G

NM_019616.3(F7):c.226-672A>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency.

Haematologica
Ferraresi, Paolo P; Balestra, Dario D; Guittard, Caroline C; Buthiau, Delphine D; Pan-Petesh, Brigitte B; Maestri, Iva I; Farah, Roula R; Pinotti, Mirko M; Giansily-Blaizot, Muriel M
Publication Date: 2020-03

Variant appearance in text: rs12431329
PubMed Link: 31273093
Variant Present in the following documents:
  • Main text
  • 1050829.pdf
View BVdb publication page