flag flag  

author = "MANNUCCI, PIER MANNUCCIO" > : "Child" (x)
1

Found 1 documents, displaying page 1 of 1

Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency

Description : Factor XIII (FXIII) deficiency is a very rare severe autosomal bleeding disorder with a frequency of 1:2,000,000 in the general population and only a few patients have been genetically characterized so far. We report a phenotype-genotype characterization of 10 unrelated Iranian patients. Two FXIII (...
Repository : Debreceni Egyetem elektronikus Archivumanak (DEA)
Language(s) : Undetermined
1

Found 1 documents, displaying page 1 of 1