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

4 Citations (Scopus)
Original languageEnglish
JournalHaemophilia
Volume18
Issue number2
DOIs
Publication statusPublished - Mar 2012

ASJC Scopus subject areas

  • Hematology
  • Genetics(clinical)

Cite this

Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency. / Bafunno, V.; Favuzzi, G.; Fierro, T.; Chetta, M.; Mastrodicasa, E.; Chinni, E.; Grandone, E.; Margaglione, M.; Gresele, P.

In: Haemophilia, Vol. 18, No. 2, 03.2012.

Research output: Contribution to journalArticle

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, vol. 18, no. 2. https://doi.org/10.1111/j.1365-2516.2011.02747.x
Bafunno, V. ; Favuzzi, G. ; Fierro, T. ; Chetta, M. ; Mastrodicasa, E. ; Chinni, E. ; Grandone, E. ; Margaglione, M. ; Gresele, P. / Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency. In: Haemophilia. 2012 ; Vol. 18, No. 2.
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