Associated Papers
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency.
Ivaskevicius V et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2010
Application of diagnostic methods and molecular diagnosis of hemoglobin disorders in Khuzestan province of Iran.
Fakher R et al.
Indian Journal of Human Genetics, 2007
Select a paper to view details