KEGG   VARIANT: 5345v1
Entry
5345v1                      Variant                                
Name
SERPINF2 mutation
Type
Loss of function
Gene
SERPINF2  serpin family F member 2 [KO:K03983]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 613168
Network
nt06514  Coagulation cascade
Disease
H00983  Alpha-2-plasmin inhibitor (a2-PI) deficiency
Reference
PMID:11472338
  Authors
Favier R, Aoki N, de Moerloose P
  Title
Congenital alpha(2)-plasmin inhibitor deficiencies: a review.
  Journal
Br J Haematol 114:4-10 (2001)
DOI:10.1046/j.1365-2141.2001.02845.x
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