Middle-aged heterozygous carriers ofWilsona€?s disease do not present with significant phenotypic deviations related to copper metabolism

A. Czlonkowska1 2; A. Wierzchowska; G. Chabik; G. Gromadzka1 2; M. Rudnicka; T. Mendel

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Middle-aged heterozygous carriers ofWilsona€?s disease do not present with significant phenotypic deviations related to copper metabolism

机译：威尔逊的中年杂合载体€€病疾病不存在与铜代谢有关的显着表型偏差

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《Journal of genetics》 |2010年第4期|共页
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A. Czlonkowska1 2; A. Wierzchowska; G. Chabik; G. Gromadzka1 2; M. Rudnicka; T. Mendel;
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1. Middle-aged heterozygous carriers of Wilson's disease do not present with signi?cant phenotypic deviations related to copper metabolism [J] . Gromadzka G., Chabik G., Mendel T., Journal of genetics . 2011,第4期

机译：威尔逊氏病的中年杂合子携带者未表现出与铜代谢有关的显着表型偏差
2. Middle-aged heterozygous carriers of Wilson’s disease do not present with significant phenotypic deviations related to copper metabolism [J] . G. Gromadzka, G. Chabik, T. Mendel, Journal of Genetics . 2010,第4期

机译：威尔逊氏病的中年杂合子携带者未表现出与铜代谢有关的明显表型偏差
3. Heterozygous tx mice have an increased sensitivity to copper loading: Implications for Wilson's disease carriers [J] . Cheah DMY, Deal YJ, Wright PFA, BioMetals: An International Journal on the Role of Metal Ions in Biology, Biochemistry and Medicine . 2007,第5期

机译：杂合tx小鼠对铜负荷的敏感性增加：对威尔逊病携带者的影响
4. Association Mapping for Compound Heterozygous Traits Using Phenotypic Distance and Integer Programming [C] . Dan Gusfield, Rasmus Nielsen International workshop on algorithms in bioinformatics . 2015

机译：表型距离和整数规划的复合杂合性状的关联图谱
5. Reproductive decisions in carriers of genetic disease: A survey of parents of children with inborn errors of metabolism [D] . Read, Catherine Yetter 2001

机译：遗传疾病携带者的生殖决策：对先天性代谢错误的儿童父母的调查
6. Whole-body and muscle protein metabolism are not affected by acute deviations from habitual protein intake in older men: the Hormonal Regulators of Muscle and Metabolism in Aging (HORMA) Study [O] . Kevin E Yarasheski, Carmen Castaneda-Sceppa, Jiaxiu He, -1

机译：老年男性习惯性蛋白质摄入的急性偏差不会影响全身和肌肉蛋白质的代谢：衰老肌肉和新陈代谢的激素调节剂（HORMA）研究
7. Risk of cardiovascular disease in double heterozygous carriers and homozygous carriers of F5 R506Q (factor V Leiden) and F2 (prothrombin) G20210A:a retrospective family cohort study [O] . Roach, Rachel E. J., Roshani, Sara, Meijer, Karina, 2011

机译：F5 R506Q（因子V Leiden）和F2（凝血酶原）G20210A的双重杂合子和纯合子携带者患心血管疾病的风险：一项回顾性家庭队列研究

Middle-aged heterozygous carriers ofWilsona€?s disease do not present with significant phenotypic deviations related to copper metabolism

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