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Article

Haemophilia B caused by mutation of a potential thrombin cleavage site in factor IX.

Nucleic acids research - 11 Mar 1990

Winship P R

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Identifiers

PMID: 2320433
DOI: 10.1093/nar/18.5.1310
PMCID: PMC330472

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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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Haemophilia B caused by mutation of a potential thrombin cleavage site in factor IX.PMID 2320433Read ↗

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An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B.Semantic proximity Read ↗

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

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