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2. Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X. Chafa O; Tagzirt M; Tapon-Bretaudière J; Reghis A; Fischer AM; LeBonniec BF Thromb Res; 2009 May; 124(1):144-8. PubMed ID: 19135706 [TBL] [Abstract][Full Text] [Related]
3. Factor X Shanghai: a mutation disrupting translocation to the endoplasmic reticulum. Asselta R Haematologica; 2005 Dec; 90(12):1590. PubMed ID: 16330428 [No Abstract] [Full Text] [Related]
4. Cloning and characterization of a cDNA encoding murine coagulation factor X. Liang Z; Cooper A; DeFord ME; Carmeliet P; Collen D; Castellino FJ; Rosen ED Thromb Haemost; 1998 Jul; 80(1):87-91. PubMed ID: 9684791 [TBL] [Abstract][Full Text] [Related]
5. Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene - Genotype-phenotype correlation in a girl with severe factor X deficiency. Hainmann I; Oldenburg J; Pavlova A; Superti-Furga A; Zieger B Hamostaseologie; 2009 May; 29(2):184-6. PubMed ID: 19404516 [TBL] [Abstract][Full Text] [Related]
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8. Factor X Nagoya 1 and Nagoya 2: a CRM- factor X deficiency and a dysfunctional CRM+ factor X deficiency characterized by substitution of Arg306 by Cys and of Gly366 by Ser, respectively. Miyata T; Kojima T; Suzuki K; Umeyama H; Yamazaki T; Kamiya T; Toyoda H; Kato H Thromb Haemost; 1998 Mar; 79(3):486-90. PubMed ID: 9531027 [TBL] [Abstract][Full Text] [Related]
9. Factor X Shanghai and disruption of translocation to the endoplasmic reticulum. Wang WB; Fu QH; Yin J; Wu WM; Ding QL; Zhou RF; Hu YQ; Wang XF; Wang ZY; Wang HL Haematologica; 2005 Dec; 90(12):1659-64. PubMed ID: 16330440 [TBL] [Abstract][Full Text] [Related]
10. Factor X Frankfurt I: molecular and functional characterization of a hereditary factor X deficiency (Gla+25 to Lys). Nöbauer-Huhmann IM; Höller W; Krinninger B; Turecek PL; Richter G; Scharrer I; Forberg E; Watzke HH Blood Coagul Fibrinolysis; 1998 Mar; 9(2):143-52. PubMed ID: 9622212 [TBL] [Abstract][Full Text] [Related]
11. [Clotting factor X deficiency resulted from an T 58-->G mutation within exon 1 of human factor X gene]. Yin J; Wang H; Wang X Zhonghua Xue Ye Xue Za Zhi; 2001 Sep; 22(9):481-3. PubMed ID: 11758231 [TBL] [Abstract][Full Text] [Related]
12. Severe FX deficiency caused by a previously unidentified 4-bp deletion compound heterozygous with a large deletion involving FVII and FX genes. Tan CW; Najm J; Morel-Kopp MC; Teo J; Chen Q; Felbor U; Ward CM Haemophilia; 2012 Mar; 18(2):e55-8. PubMed ID: 22126652 [No Abstract] [Full Text] [Related]
13. Characterization of porcine factor VII, X and comparison with human factor VII, X. Chen Y; Qiao J; Tan W; Lu Y; Qin S; Zhang J; Li S; Bu H; Cheng J Blood Cells Mol Dis; 2009; 43(1):111-8. PubMed ID: 19286401 [TBL] [Abstract][Full Text] [Related]
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