Hereditary protein C deficiency caused by the compound heterozygous mutations, Gly 282 Ser and Met 364 Ile ; Contribution of each protein C mutation on pathogenesis of thrombosis
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2008 ◽
Vol 123
(2)
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pp. 412-417
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1993 ◽
Vol 70
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pp. 636-641
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1994 ◽
Vol 72
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pp. 814-818
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2014 ◽
Vol 13
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pp. 2969-2977
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2010 ◽
Vol 52
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pp. 489-493
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2018 ◽
Vol 29
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pp. 216-219
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