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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

MCVEY, JH, IMANAKA, Y, NISHIMURA, T, OBRIEN, DP, BOLTONMAGGS, PHB and TUDDENHAM, EGD (1995) 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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Item Type: Conference or Workshop Item (UNSPECIFIED)
Authors :
NameEmailORCID
MCVEY, JHj.mcvey@surrey.ac.ukUNSPECIFIED
IMANAKA, YUNSPECIFIEDUNSPECIFIED
NISHIMURA, TUNSPECIFIEDUNSPECIFIED
OBRIEN, DPUNSPECIFIEDUNSPECIFIED
BOLTONMAGGS, PHBUNSPECIFIEDUNSPECIFIED
TUDDENHAM, EGDUNSPECIFIEDUNSPECIFIED
Date : 1 June 1995
Contributors :
ContributionNameEmailORCID
publisherF K SCHATTAUER VERLAG GMBH, UNSPECIFIEDUNSPECIFIED
Uncontrolled Keywords : Science & Technology, Life Sciences & Biomedicine, Hematology, Peripheral Vascular Disease, Cardiovascular System & Cardiology, HEMATOLOGY, PERIPHERAL VASCULAR DISEASE
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 09:59
Last Modified : 17 May 2017 14:46
URI: http://epubs.surrey.ac.uk/id/eprint/825894

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