A NEW HOMOZYGOUS MUTATION (GLU19ALA) IN THE GLA DOMAIN CAUSES A CRMRED SYMPTOMATIC FACTOR-X DEFICIENCY

Authors
CINOTTI S FIORINI S LUNGHI B MARCHETTI G LONGO G MORFINI M BERNARDI F
Citation
S. Cinotti et al., A NEW HOMOZYGOUS MUTATION (GLU19ALA) IN THE GLA DOMAIN CAUSES A CRMRED SYMPTOMATIC FACTOR-X DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 1616-1616
Citations number
NO
Categorie Soggetti
Hematology,"Peripheal Vascular Diseas
Journal title
Thrombosis and haemostasis → ACNP
ISSN journal
03406245
Year of publication
1997
Supplement
S
Pages
1616 - 1616
Database
ISI
SICI code
0340-6245(1997):<1616:ANHM(I>2.0.ZU;2-I