High frequency of C4 "null" alleles in primary antiphospholipid syndrome
Ann Med Interne (Paris)
.
1996;147(2):115-6.
Authors
S Bentolila
,
V Fremeaux-Bacchi
,
L Weiss
,
J Blouin
,
M D Kazatchkine
,
J C Piette
PMID:
8760690
No abstract available
MeSH terms
Adult
Antiphospholipid Syndrome / genetics*
Complement C4 / genetics*
Disease Susceptibility
Female
Humans
Male
Middle Aged
Phenotype
Substances
Complement C4