A novel protein C mutation causing neonatal purpura fulminans
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s13312-016-0981-2.pdf
Reference9 articles.
1. Goldenberg NA, Manco-Johnson MJ. Protein C deficiency Haemophilia. 2008;14:1214–21.
2. Knoebl PN. Severe congenital protein C deficiency: the use of protein C concentrates (human) as replacement therapy for life-threatening blood-clotting complications. Biol Targets Ther. 2008;2:285–96.
3. Price VE, Ledingham DL, Krümpel A, Chan AK. Diagnosis and management of neonatal purpura fulminans. Semin Fetal Neonatal Med. 2011;16:318–22.
4. Lind B, van Solinge WW, Schwartz M, Thorsen S. Splice site mutation in the human protein C gene associated with venous thrombosis: demonstration of exon skipping by ectopic transcript analysis. Blood. 1993;82:2423–32.
5. Kirkinen P, Salonvaara M, Nikolajev K, Vanninen R, Heinonen K. Antepartum findings in fetal protein C deficiency. Prenat Diagn. 2000;20:746–9.
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