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GENATLAS PHENOTYPE

last update : 30/06/2006

Symbol	F13B
Location	1q31
Name	fibrin-stabilizing factor deficiency, type I
Corresponding gene	F13B
Main clinical features	bleeding tendency, defective wound healing, habitual abortion
Genetic determination
Function/system disorder	hematology
Type	disease

Gene product

Name	coagulation factor XIII, B polypeptide (F13B)