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Combination of congenital coagulation disorders: Factor II gene mutation G20210A, Factor V Leiden gene mutation G1691A and protein S deficiency. a family study.

Haematologica - 1 Jun 2003

González Cocaño M C, Díaz-Golpe V, Martín S, Sánchez Del Real J, Redondo M C

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 12801853

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Combination of congenital coagulation disorders: Factor II gene mutation G20210A, Factor V Leiden gene mutation G1691A and protein S deficiency. a family study.PMID 12801853Read ↗

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