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The CDC Hemophilia B mutation project mutation list: a new online resource
Hemophilia B (HB) is caused by mutations in the human gene F9. The mutation type plays a pivotal role in genetic counseling and prediction of inhibitor development. To help the HB community understand the molecular etiology of HB, we have developed a listing of all F9 mutations that are reported to...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Blackwell Publishing Ltd
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3865591/ https://ncbi.nlm.nih.gov/pubmed/24498619 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.30 |
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