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Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis

Simmonds, RE, Ireland, H, Kunz, G, Lane, DA, Bhavnani, M, Castaman, G, Hambley, H, Laffan, M, OConnor, N, Sas, G, Tew, CJ and Walker, ID (1996) Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis BLOOD, 88 (11). pp. 4195-4204.

Full text not available from this repository.
Item Type: Article
Authors :
NameEmailORCID
Simmonds, RErachel.simmonds@surrey.ac.ukUNSPECIFIED
Ireland, HUNSPECIFIEDUNSPECIFIED
Kunz, GUNSPECIFIEDUNSPECIFIED
Lane, DAUNSPECIFIEDUNSPECIFIED
Bhavnani, MUNSPECIFIEDUNSPECIFIED
Castaman, GUNSPECIFIEDUNSPECIFIED
Hambley, HUNSPECIFIEDUNSPECIFIED
Laffan, MUNSPECIFIEDUNSPECIFIED
OConnor, NUNSPECIFIEDUNSPECIFIED
Sas, GUNSPECIFIEDUNSPECIFIED
Tew, CJUNSPECIFIEDUNSPECIFIED
Walker, IDUNSPECIFIEDUNSPECIFIED
Date : 1 December 1996
Uncontrolled Keywords : Science & Technology, Life Sciences & Biomedicine, Hematology, HEMATOLOGY, ANDROGEN-BINDING PROTEIN, C4B-BINDING PROTEIN, VENOUS THROMBOSIS, POINT MUTATIONS, NEUTRAL DIMORPHISM, BLOOD-COAGULATION, FUNCTIONAL ASSAY, ALPHA PROS1, PS-ALPHA, CDNA
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 10:37
Last Modified : 17 May 2017 14:51
URI: http://epubs.surrey.ac.uk/id/eprint/828532

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