Family studies in Scott syndrome
- PMID: 9207489
Family studies in Scott syndrome
Comment on
-
Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder.Blood. 1996 Feb 15;87(4):1409-15. Blood. 1996. PMID: 8608230
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
