Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12857/124863
Title: Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)
Authors: Girolami, Antonio 
Minoldo, Salvador
Ferrari, Silvia 
Colussi, Diego
Lombardi, Anna Maria 
Guglielmone, Hugo
Keywords: FX deficiency;menorrhagia;new mutation;plasma;polymorphism;potentiating effect
Mesh headings: Factor X;Factor X Deficiency;Mutation, Missense
Secondary Mesh headings: Adult;Blood Coagulation;Female;Heterozygote;Humans;Male;Models, Molecular;Pedigree;Protein Conformation
Issue Date: 2017
Journal: Cardiovascular & hematological disorders drug targets 
Abstract: 
The aim was to report a new family with congenital FX deficiency.
URI: http://hdl.handle.net/20.500.12857/124863
ISSN: 1871529X
DOI: 10.2174/1871529X17666170908105839
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