Successful liver transplantation for homozygous protein C deficiency with a type II mutation using a heterozygous living related donor

Author:

Boucher Alexander A.1ORCID,Luchtman-Jones Lori1,Nathan Jaimie D.2,Palumbo Joseph S.1

Affiliation:

1. Division of Hematology; Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine; Cincinnati Ohio

2. Division of General & Thoracic Surgery, Department of Pediatrics; Cincinnati Children's Hospital Medical Center; Cincinnati Ohio

Publisher

Wiley

Subject

Hematology

Reference26 articles.

1. Protein C deficiency caused by a novel mutation in the PROC gene in an infant with delayed onset purpura fulminans;Al Harbi;Case Rep Dermatol Med.,2017

2. The protein C pathway;Esmon;Chest.,2003

3. Protein C deficiency;Goldenberg;Haemophilia.,2008

4. Studies on congenital protein C deficiency in Japanese: prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases;Sakata;Semin Thromb Hemost.,2000

5. Absence of thrombosis in subjects with heterozygous protein C deficiency;Miletich;N Engl J Med.,1987

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