[Combined abnormalities of plasminogen abnormality, von Willebrand disease, hypofibrinogenemia and increased erythrocyte membrane fragility. A new hereditary syndrome?]
Rinsho Ketsueki
.
1986 May;27(5):730-7.
[Article in Japanese]
Authors
K Shinmyozu
,
Y Maruyama
,
M Osame
,
A Igata
,
H Fukusako
,
M Tara
PMID:
3489113
No abstract available
Publication types
English Abstract
MeSH terms
Adult
Afibrinogenemia / complications*
Afibrinogenemia / genetics
Humans
Male
Osmotic Fragility*
Plasminogen / analysis*
von Willebrand Diseases / complications*
von Willebrand Diseases / genetics
Substances
Plasminogen