Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B Leyden.
Hemophilia B Leyden is an X chromosome-linked bleeding disorder characterized by very low plasma levels of blood coagulation factor IX (fIX) during childhood. After puberty, plasma fIX levels gradually rise to a maximum of 60% of normal, probably under the influence of testosterone. Single point mut...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1992
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC49488/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1631121/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.89.14.6300 |
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