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Article

Identification of a factor IX point mutation using SSCP analysis and direct sequencing.

Nucleic acids research - 25 Sept 1990

Demers D B, Odelberg S J, Fisher L M

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 2216751
DOI: 10.1093/nar/18.18.5575
PMCID: PMC332266

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a factor IX point mutation using SSCP analysis and direct sequencing.PMID 2216751Read ↗

Identification of twenty-one new mutations in the factor IX gene by SSCP analysis.Semantic proximity Read ↗

Screening for mutations in the gene encoding factor IX.Semantic proximity Read ↗

Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing.Semantic proximity Read ↗

Factor IX mutations: rapid, direct screening methods for 20 new families with hemophilia 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 and functional basis of hereditary factor IX defects.Semantic proximity Read ↗

Seven novel mutations in carbonic anhydrase II deficiency syndrome identified by SSCP and direct sequencing analysis.Semantic proximity Read ↗

Remembrances of factor VIII. Part 2: the path to mutation discovery.Semantic proximity Read ↗

Seven novel point mutations in the F11 gene in Iranian FXI-deficient patients.Semantic proximity Read ↗

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

Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivity.Semantic proximity Read ↗

Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency.Semantic proximity Read ↗

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