Factor XIII deficiency

[1] AESCHLIMANN D, 1994, THROMB HAEMOSTASIS, V71, P402

[2] Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency: effects of these mutations on FXIIIA RNA processing and protein structure [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (02) : 425 - 428

[3] Anwar R, 1998, THROMB HAEMOSTASIS, V79, P1151

[4] MOLECULAR-BASIS OF INHERITED FACTOR-XIII DEFICIENCY - IDENTIFICATION OF MULTIPLE MUTATIONS PROVIDES INSIGHTS INTO PROTEIN FUNCTION [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1995, 91 (03) : 728 - 735

[5] Identification of a large deletion, spanning exons 4 to 11 of the human factor XIIIA gene, in a factor XIII-deficient family [J]. BLOOD, 1998, 91 (01) : 149 - 153

[6] Genotype/phenotype correlations for coagulation factor XIII: Specific normal polymorphisms are associated with high or low factor XIII specific activity [J]. BLOOD, 1999, 93 (03) : 897 - 905

[7] AOKI N, 1980, BLOOD, V55, P483

[8] FACTOR-XIII(A CALGARY) - A CANDIDATE MISSENSE MUTATION (LEU667PRO) IN THE BETA-BARREL 2 DOMAIN OF THE FACTOR-XIII(A) SUBUNIT [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1995, 91 (02) : 452 - 457

[9] Aslam S, 1996, AM J HEMATOL, V53, P77, DOI 10.1002/(SICI)1096-8652(199610)53:2<77::AID-AJH4>3.3.CO

[10] 2-2

[1] AESCHLIMANN D, 1994, THROMB HAEMOSTASIS, V71, P402

[2] Splicing and missense mutations in the human FXIIIA gene causing FXIII deficiency: effects of these mutations on FXIIIA RNA processing and protein structure [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (02) : 425 - 428

[3] Anwar R, 1998, THROMB HAEMOSTASIS, V79, P1151

[4] MOLECULAR-BASIS OF INHERITED FACTOR-XIII DEFICIENCY - IDENTIFICATION OF MULTIPLE MUTATIONS PROVIDES INSIGHTS INTO PROTEIN FUNCTION [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1995, 91 (03) : 728 - 735

[5] Identification of a large deletion, spanning exons 4 to 11 of the human factor XIIIA gene, in a factor XIII-deficient family [J]. BLOOD, 1998, 91 (01) : 149 - 153

[6] Genotype/phenotype correlations for coagulation factor XIII: Specific normal polymorphisms are associated with high or low factor XIII specific activity [J]. BLOOD, 1999, 93 (03) : 897 - 905

[7] AOKI N, 1980, BLOOD, V55, P483

[8] FACTOR-XIII(A CALGARY) - A CANDIDATE MISSENSE MUTATION (LEU667PRO) IN THE BETA-BARREL 2 DOMAIN OF THE FACTOR-XIII(A) SUBUNIT [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1995, 91 (02) : 452 - 457

[9] Aslam S, 1996, AM J HEMATOL, V53, P77, DOI 10.1002/(SICI)1096-8652(199610)53:2<77::AID-AJH4>3.3.CO

[10] 2-2