An Sp1 binding site mutation of the PROSl promoter in a patient with protein S deficiency.

An Sp1 binding site mutation of the PROSl promoter in a patient with protein S deficiency.
复制标题

蛋白S缺陷患者中PROS1启动子的Sp1结合位点突变。

DOI:
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发表时间:
2007
期刊:
Br J Haematol 138
影响因子:
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通讯作者:
et. al.
et. al.
中科院分区:
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文献类型:
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作者:
N. Sanda;T. Kojima;et. al.

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