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Article

[Analysis of a single nucleotide deletion responsible for congenital plasmin inhibitor deficiency].

[Rinsho ketsueki] The Japanese journal of clinical hematology - 1 Jan 2004

Nakahara Masako

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PMID: 14999928

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[Analysis of a single nucleotide deletion responsible for congenital plasmin inhibitor deficiency].PMID 14999928Read ↗

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[Congenital lactase deficiency: Identification of a new mutation].Semantic proximity Read ↗

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A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency.Semantic proximity Read ↗

[Structural and functional analysis of mutant blood coagulation and fibrinolytic factors].Semantic proximity Read ↗

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[Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis].Semantic proximity Read ↗

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