Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency

V. Bafunno, G. Favuzzi, T. Fierro, M. Chetta, E. Mastrodicasa, E. Chinni, E. Grandone, M. Margaglione, P. Gresele

Research output: Contribution to journalArticle

Original languageEnglish
JournalHaemophilia
Volume18
Issue number2
DOIs
Publication statusPublished - Mar 2012

ASJC Scopus subject areas

  • Hematology
  • Genetics(clinical)

Cite this

Bafunno, V., Favuzzi, G., Fierro, T., Chetta, M., Mastrodicasa, E., Chinni, E., Grandone, E., Margaglione, M., & Gresele, P. (2012). Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency. Haemophilia, 18(2). https://doi.org/10.1111/j.1365-2516.2011.02747.x