Address
:
[go:
up one dir
,
main page
]
Include Form
Remove Scripts
Accept Cookies
Show Images
Show Referer
Rotate13
Base64
Strip Meta
Strip Title
Session Cookies
VARIANT: 2159v1
Help
Entry
2159v1 Variant
Name
F10 mutation
Gene
F10
coagulation factor X [KO:
K01314
]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar:
613872
Network
nt06514
Coagulation cascade
Disease
H02257
Factor X deficiency
Reference
PMID:
12127953
Authors
Uprichard J, Perry DJ
Title
Factor X deficiency.
Journal
Blood Rev 16:97-110 (2002)
DOI:
10.1054/blre.2002.0191
LinkDB
All DBs
DBGET
integrated database retrieval system