Characterization of factor IX defects in hemophilia B patients.
about
The factor VIII C1 domain contributes to platelet bindingHaemophilia B (sixth edition): a database of point mutations and short additions and deletionsHaemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994.CRISPR/Cas9-mediated somatic correction of a novel coagulator factor IX gene mutation ameliorates hemophilia in mouse.Review of the Target-Specific Oral Anticoagulants in Development for the Treatment and Prevention of Venous Thromboembolism.A domain mutations in 65 haemophilia A families and molecular modelling of dysfunctional factor VIII proteins.Consequences of factor IX mutations in 26 families with haemophilia B.New anticoagulants for venous thromboembolism and atrial fibrillation: what the future holds.Nuclease-Mediated Gene Therapies for Inherited Metabolic Diseases of the Liver.
P2860
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P2860
Characterization of factor IX defects in hemophilia B patients.
description
1993 nî lūn-bûn
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1993年の論文
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年学术文章
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1993年學術文章
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1993年學術文章
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name
Characterization of factor IX defects in hemophilia B patients.
@en
Characterization of factor IX defects in hemophilia B patients.
@nl
type
label
Characterization of factor IX defects in hemophilia B patients.
@en
Characterization of factor IX defects in hemophilia B patients.
@nl
prefLabel
Characterization of factor IX defects in hemophilia B patients.
@en
Characterization of factor IX defects in hemophilia B patients.
@nl
P921
P1476
Characterization of factor IX defects in hemophilia B patients.
@en
P2093
P304
P356
10.1016/0076-6879(93)22011-4
P407
P577
1993-01-01T00:00:00Z