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Article

Screening for mutations in the gene encoding factor IX.

Journal of inherited metabolic disease - 1 Jan 1992

Nielsen L R, Schwartz M, Scheibel E

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 1357229
DOI: 10.1007/BF02435971

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening for mutations in the gene encoding factor IX.PMID 1357229Read ↗

Molecular and functional basis of hereditary factor IX defects.Semantic proximity Read ↗

Identification of a factor IX point mutation using SSCP analysis and direct sequencing.Semantic proximity Read ↗

Factor IX mutations: rapid, direct screening methods for 20 new families with hemophilia B.Semantic proximity Read ↗

Twenty-five novel mutations of the factor IX gene in haemophilia B.Semantic proximity Read ↗

Clinical significance of two mutations in the factor IX gene in a family with haemophilia B.Semantic proximity Read ↗

Identification of four novel mutations in the factor VIII gene: three missense mutations (E1875G, G2088S, I2185T) and a 2-bp deletion (1780delTC).Semantic proximity Read ↗

Molecular analysis of severe factor XI deficiency in three Italian patients.Semantic proximity Read ↗

Analysis of Hereditary FXII Deficiency Caused by Three Mutations Including a Novel MutationSemantic proximity Read ↗

Haemophilia B and factor IX mutations.Semantic proximity Read ↗

Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family.Semantic proximity Read ↗

First molecular characterization of a patient with combined factor V and factor VII deficiency.Semantic proximity Read ↗

Factor IX polypyrimidine tract mutation analysis using mRNA from peripheral blood leukocytes.Semantic proximity Read ↗

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