Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene.
about
Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutationsThe molecular basis of quantitative fibrinogen disorders.Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins.Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia.Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen v
P2860
Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain gene.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh-hant
name
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@en
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@nl
type
label
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@en
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@nl
prefLabel
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@en
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@nl
P2093
P50
P1476
Congenital afibrinogenemia: in ...... e fibrinogen Bbeta-chain gene.
@en
P2093
Maria Luisa Tenchini
Massimo Malcovati
Silvia Spena
P356
10.1016/S0925-4439(03)00125-X
P577
2003-10-01T00:00:00Z