Fig. 1From: A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1Family map. In the family map of hereditary protein S deficiency, the proband (III5) and other patients carry a c. 1820T > C (p.Leu607Ser) PROS1 heterozygous mutationBack to article page