KEGG   VARIANT: 3818v1
Entry
3818v1                      Variant                                
Name
KLKB1 mutation
Type
Loss of function
Gene
KLKB1  kallikrein B1 [KO:K01324]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 229000
Network
nt06514  Coagulation cascade
Disease
H01078  Fletcher factor deficiency
Reference
PMID:21091145
  Authors
Girolami A, Scarparo P, Candeo N, Lombardi AM
  Title
Congenital prekallikrein deficiency.
  Journal
Expert Rev Hematol 3:685-95 (2010)
DOI:10.1586/ehm.10.69
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