IDENTIFICATION OF A NOVEL MECHANISM OF HUMAN GENETIC-DISEASE - A MISSENSE MUTATION CAUSING FXI DEFICIENCY THROUGH A CHANGE IN MESSENGER-RNA STABILITY

JH MCVEY; Y IMANAKA; T NISHIMURA; DP OBRIEN; PHB BOLTONMAGGS; EGD TUDDENHAM

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IDENTIFICATION OF A NOVEL MECHANISM OF HUMAN GENETIC-DISEASE - A MISSENSE MUTATION CAUSING FXI DEFICIENCY THROUGH A CHANGE IN MESSENGER-RNA STABILITY

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IDENTIFICATION OF A NOVEL MECHANISM OF HUMAN GENETIC-DISEASE - A MISSENSE MUTATION CAUSING FXI DEFICIENCY THROUGH A CHANGE IN MESSENGER-RNA STABILITY

JH MCVEY, Y IMANAKA, T NISHIMURA, DP OBRIEN, PHB BOLTONMAGGS and EGD TUDDENHAM

THROMBOSIS AND HAEMOSTASIS, Vol.73(6), pp.1442-1442

01/06/1995

Abstract

Science & Technology

Life Sciences & Biomedicine

Hematology

Peripheral Vascular Disease

Cardiovascular System & Cardiology

HEMATOLOGY

PERIPHERAL VASCULAR DISEASE

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Title: IDENTIFICATION OF A NOVEL MECHANISM OF HUMAN GENETIC-DISEASE - A MISSENSE MUTATION CAUSING FXI DEFICIENCY THROUGH A CHANGE IN MESSENGER-RNA STABILITY
Creators: JH MCVEY
Y IMANAKA
T NISHIMURA
DP OBRIEN
PHB BOLTONMAGGS
EGD TUDDENHAM
Contributors: F K SCHATTAUER VERLAG GMBH (Publisher)
Publication Details: THROMBOSIS AND HAEMOSTASIS, Vol.73(6), pp.1442-1442
Date published: 01/06/1995
Date submitted: 17/05/2017
Identifiers: 99515159302346
Academic Unit: University of Surrey
Resource Type: Conference presentation

IDENTIFICATION OF A NOVEL MECHANISM OF HUMAN GENETIC-DISEASE - A MISSENSE MUTATION CAUSING FXI DEFICIENCY THROUGH A CHANGE IN MESSENGER-RNA STABILITY

Abstract

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