Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients.

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Early prediction of postoperative liver dysfunction and clinical outcome using antithrombin III-activity Gene analysis of inherited antithrombin deficiency and functional analysis of abnormal antithrombin protein (N87D).

P2860

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Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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Causative genetic mutations fo ...... round among Japanese patients.

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Causative genetic mutations fo ...... round among Japanese patients.

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Causative genetic mutations fo ...... round among Japanese patients.

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Causative genetic mutations fo ...... round among Japanese patients.

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Causative genetic mutations fo ...... ground among Japanese patients

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Daisuke Yamaguchi

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Eriko Morishita

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Fumina Taniguchi

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Haruka Nakano

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Hidesaku Asakura

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Mao Takata

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Miho Hanamura

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Sayaka Kamijima

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Shigeki Ohtake

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Shiori Katsu

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P2860

VTE, thrombophilia, antithrombotic therapy, and pregnancy: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines

The anticoagulant activation of antithrombin by heparin

Molecular genetics of antithrombin deficiency.

Identification of critical molecular interactions mediating heparin activation of antithrombin: implications for the design of improved heparin anticoagulants.

Antithrombin III deficiency in Indian patients with deep vein thrombosis: identification of first India based AT variants including a novel point mutation (T280A) that leads to aggregation.

Antithrombin III Toyama: replacement of arginine-47 by cysteine in hereditary abnormal antithrombin III that lacks heparin-binding ability.

Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population.

ACOG Practice Bulletin No. 138: Inherited thrombophilias in pregnancy.

Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis.

Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.

P2888

s12185-016-2142-8

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287-294

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scholarly article

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105

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Akiko Sekiya

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2016-11-17T00:00:00Z

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27858332

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Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients.

about

P2860

P2860

Causative genetic mutations for antithrombin deficiency and their clinical background among Japanese patients.

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