Fig. 2.
Pedigree of the FXIII-deficient family studied. The inheritance pattern of the Arg408Gln, CGG → CAG mutation identified is presented. The father is homozygous normal at this sequence.

Pedigree of the FXIII-deficient family studied. The inheritance pattern of the Arg408Gln, CGG → CAG mutation identified is presented. The father is homozygous normal at this sequence.

Close Modal
This Feature Is Available To Subscribers Only

or Create an Account

Close Modal
Close Modal