Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.

W Renner; H Köppel; M Brodmann; E Pabst; Katharina Schallmoser; H Toplak; T C Wascher; E Pilger

Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.

W Renner, H Köppel, M Brodmann, E Pabst, Katharina Schallmoser (Co-Autor/-in), H Toplak, T C Wascher, E Pilger

Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

27 Quellenangaben (Web of Science)

Originalsprache	Englisch
Seiten (von - bis)	20-22
Fachzeitschrift	THROMBOSIS AND HAEMOSTASIS
Jahrgang	83
Ausgabenummer	1
Publikationsstatus	Veröffentlicht - 2000

Dieses zitieren

Renner, W., Köppel, H., Brodmann, M., Pabst, E., Schallmoser, K., Toplak, H., Wascher, T. C., & Pilger, E. (2000). Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease. THROMBOSIS AND HAEMOSTASIS , 83(1), 20-22.

Renner, W ; Köppel, H ; Brodmann, M et al. / Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease. in: THROMBOSIS AND HAEMOSTASIS 2000 ; Jahrgang 83, Nr. 1. S. 20-22.

@article{6cdad149afaf4d2a93b301e4dfcb9a93,

title = "Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.",

keywords = "ACTIVATED PROTEIN-C, COAGULATION-FACTOR-V, MYOCARDIAL-INFARCTION, PROTHROMBIN GENE, VENOUS THROMBOSIS, VASCULAR-DISEASE, YOUNG-WOMEN, RISK FACTOR, RESISTANCE, PREVALENCE",

author = "W Renner and H K{\"o}ppel and M Brodmann and E Pabst and Katharina Schallmoser and H Toplak and Wascher, \{T C\} and E Pilger",

year = "2000",

language = "English",

volume = "83",

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journal = "THROMBOSIS AND HAEMOSTASIS ",

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Renner, W, Köppel, H, Brodmann, M, Pabst, E, Schallmoser, K, Toplak, H, Wascher, TC & Pilger, E 2000, 'Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.', THROMBOSIS AND HAEMOSTASIS , Jg. 83, Nr. 1, S. 20-22.

Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease. / Renner, W; Köppel, H; Brodmann, M et al.
in: THROMBOSIS AND HAEMOSTASIS , Jahrgang 83, Nr. 1, 2000, S. 20-22.

Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

TY - JOUR

T1 - Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.

AU - Renner, W

AU - Köppel, H

AU - Brodmann, M

AU - Pabst, E

AU - Schallmoser, Katharina

AU - Toplak, H

AU - Wascher, T C

AU - Pilger, E

PY - 2000

Y1 - 2000

KW - ACTIVATED PROTEIN-C

KW - COAGULATION-FACTOR-V

KW - MYOCARDIAL-INFARCTION

KW - PROTHROMBIN GENE

KW - VENOUS THROMBOSIS

KW - VASCULAR-DISEASE

KW - YOUNG-WOMEN

KW - RISK FACTOR

KW - RESISTANCE

KW - PREVALENCE

M3 - Original Article

C2 - 10669148

SN - 0340-6245

VL - 83

SP - 20

EP - 22

JO - THROMBOSIS AND HAEMOSTASIS

JF - THROMBOSIS AND HAEMOSTASIS

IS - 1

ER -

Renner W, Köppel H, Brodmann M, Pabst E, Schallmoser K, Toplak H et al. Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease. THROMBOSIS AND HAEMOSTASIS . 2000;83(1):20-22.