KEGG   VARIANT: 2165v1
Entry
2165v1                      Variant                                
Name
F13B mutation
Type
Loss of function
Gene
F13B  coagulation factor XIII B chain [KO:K03906]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 134580
Network
nt06514  Coagulation cascade
Disease
H00945  Factor XIII deficiency
Reference
PMID:19141159
  Authors
Hsieh L, Nugent D
  Title
Factor XIII deficiency.
  Journal
Haemophilia 14:1190-200 (2008)
DOI:10.1111/j.1365-2516.2008.01857.x
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