机译:并存的假性黄原瘤弹性蛋白和维生素K依赖性凝血因子缺乏症:复合杂合性的GGCX基因突变。
From the Department of Dermatology and Cutaneous Biology,Jefferson Medical College and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania;
the Cardiovascular Research Institute and VitaK,University of Maastricht, The Netherlands;
the Office of the Clinical Director,National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland;
the Pediatric Tumor Biology and Ultrastructural Pathology Section,Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
From the Department of Dermatology and Cutaneous Biology,Jefferson Medical College and Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania;
and the Dermatology Branch,Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland;
机译:弹性假黄瘤和维生素K依赖性凝血因子缺乏症共存:GGCX基因突变的复合杂合性。
机译:具有凝血缺陷的假瘤型蛋白样患者的表征,皮肤辅病和GGCX化合物杂合性
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
机译:第一种化合物IERERSozygoslty在γ-谷氨酰羧化酶基因中引起所有豚素k依赖性血液凝血因子的组合缺陷
机译:4-硝基喹啉-1-氧化物诱导的Ha-ras点突变与杂合性丧失,基因扩增和基因组不稳定有关。
机译:并存的假性假黄瘤弹性蛋白和维生素K依赖性凝血因子缺乏症
机译:并存的假性黄原瘤弹性蛋白和维生素K依赖性凝血因子缺乏症:GGCX基因突变的复合杂合性。