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Homozygosity Mapping of a Second Gene Locus for Hereditary Combined Deficiency of Witamin K-Dependent Clotting Factors (FMFD) to Chromosome 16

机译：用于血液磷酸血栓缺乏的第二基因遗迹的纯合理映射到染色体16

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Familial multiple coagulation factor deficiency (FMFD) of factors II, VII, IX, X, protein C and protein S is a very rare bleeding disorder with autosomal recessive inheritance [1]. The disease may result either from a defective resorption/transport of vitamin K to the liver, or from a mutation in one of the genes encoding gamma-carboxylase (GGCX) or other proteins of the Vitamin K 2,3-epoxide reductase (VKOR, Fig. 1) [2,3].

机译：家族性多种凝血因子缺乏（FMFD）因子II，VII，IX，X，蛋白C和蛋白质是一种非常罕见的出血障碍，具有常染色体隐性遗传[1]。该疾病可能导致维生素K的缺陷再吸收/转运到肝脏，或从编码γ-羧化酶（GGCX）的基因中的突变或维生素K 2,3-环氧化还原酶的其他蛋白质（VKOR，图1）[2,3]。

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《Hemophilie-Symposion》|2004年||共5页
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A. Fregin; S. Rost; W. Wolz; A. Krebsgva; C.R. Muller; J. Oldenburg;
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中图分类出血性疾病;
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1. Effective hemostasis during minor surgery in a case of hereditary combined deficiency of vitamin K-dependent clotting factors. [J] . Lapecorella M, Napolitano M, Bernardi F, Clinical and applied thrombosis/hemostasis . 2010,第2期

机译：遗传性维生素K依赖性凝血因子缺乏综合症的情况下，在小手术中有效止血。
2. Hereditary combined deficiency of the vitamin K-dependent clotting factors [J] . Mariasanta Napolitano, Guglielmo Mariani, Mario Lapecorella Orphanet journal of rare diseases . 2010,第S1期

机译：遗传性缺乏维生素K依赖性凝血因子
3. Congenital Combined Deficiency of the Vitamin K-dependent Clotting Factors (VKCFD): A Novel Gamma-glutamyl Carboxylase (GGCX) Mutation [J] . Al Absi Hebah S., Abdullah Mohammad F. Journal of pediatric hematology/oncology: Official journal of the American Society of Pediatric Hematology/Oncology . 2019,第4期

机译：先天性组合缺乏维生素K依赖性凝血因子（VKCFD）：一种新型γ-谷氨酸羧化酶（GGCX）突变
4. Homozygosity Mapping of a Second Gene Locus for Hereditary Combined Deficiency of Witamin K-Dependent Clotting Factors (FMFD) to Chromosome 16 [C] . A. Fregin, S. Rost, W. Wolz, Hemophilie-Symposion . 2004

机译：用于血液磷酸血栓缺乏的第二基因遗迹的纯合理映射到染色体16
5. Development of a map-based cloning system in Sorghum bicolor: 1. Isolation of megabase-size DNA and construction of a bacterial artificial chromosome library and 2. Genetic and physical mapping of the 5S rDNA locus. [D] . Woo, Sung-Sick. 1996

机译：双色高粱基于图谱的克隆系统的开发：1.分离碱基大小庞大的DNA和构建细菌人工染色体文库，以及2. 5S rDNA基因座的遗传和物理作图。
6. Hereditary combined deficiency of the vitamin K-dependent clotting factors [O] . Mariasanta Napolitano, Guglielmo Mariani, Mario Lapecorella 2010

机译：遗传性维生素K依赖性凝血因子缺乏症
7. Hereditary combined deficiency of the vitamin K-dependent clotting factors [O] . Napolitano, M, Mariani, G, Lapecorella, M 2010

机译：遗传性维生素K依赖性凝血因子缺乏症

Homozygosity Mapping of a Second Gene Locus for Hereditary Combined Deficiency of Witamin K-Dependent Clotting Factors (FMFD) to Chromosome 16

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