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: 2266v1
Help
Entry
2266v1 Variant
Name
FGG mutation
Gene
FGG
fibrinogen gamma chain [KO:
K03905
]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar:
134850
Network
nt06514
Coagulation cascade
Disease
H00222
Afibrinogenemia
Reference
PMID:
32623564
Authors
Zhang Y, Zhang Z, Shu S, Niu W, Xie W, Wan J, Zhai Z, Wang C
Title
The genetics of venous thromboembolism: a systematic review of thrombophilia families.
Journal
J Thromb Thrombolysis 51:359-369 (2021)
DOI:
10.1007/s11239-020-02203-7
Reference
PMID:
16855369
Authors
Neerman-Arbez M
Title
Molecular basis of fibrinogen deficiency.
Journal
Pathophysiol Haemost Thromb 35:187-98 (2006)
DOI:
10.1159/000093566
LinkDB
All DBs
DBGET
integrated database retrieval system