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. 1989 May 11;17(9):3614. doi: 10.1093/nar/17.9.3614

A Dutch family with moderately severe hemophilia B (factor IXHeerde) has a missense mutation identical to that of factor IX London 2.

S R Poort ¹, E Briët ¹, R M Bertina ¹, P H Reitsma ¹

PMCID: PMC317825 PMID: 2726505

Abstract

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Barker D., Schafer M., White R. Restriction sites containing CpG show a higher frequency of polymorphism in human DNA. Cell. 1984 Jan;36(1):131–138. doi: 10.1016/0092-8674(84)90081-3. [DOI] [PubMed] [Google Scholar]
Reitsma P. H., Bertina R. M., Ploos van Amstel J. K., Riemens A., Briët E. The putative factor IX gene promoter in hemophilia B Leyden. Blood. 1988 Sep;72(3):1074–1076. [PubMed] [Google Scholar]

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