Gamma371 Thr-->Ile substitution in the fibrinogen gammaD domain causes hypofibrinogenaemia.
about
Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutationsA novel fibrinogen variant--Praha I: hypofibrinogenemia associated with gamma Gly351Ser substitution.The molecular basis of quantitative fibrinogen disorders.Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.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
Gamma371 Thr-->Ile substitution in the fibrinogen gammaD domain causes hypofibrinogenaemia.
description
2001 nî lūn-bûn
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2001年の論文
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2001年学术文章
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2001年学术文章
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2001年学术文章
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name
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@en
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@nl
type
label
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@en
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@nl
prefLabel
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@en
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@nl
P2093
P1476
Gamma371 Thr-->Ile substitutio ...... in causes hypofibrinogenaemia.
@en
P2093
A P Fellowes
D A Triplett
P M George
S O Brennan
P304
P356
10.1016/S0167-4838(01)00280-1
P577
2001-12-01T00:00:00Z