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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Detalles Bibliográficos
Autores principales: Li, Tengguo, Miller, Connie H, Payne, Amanda B, Craig Hooper, W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865591/
https://www.ncbi.nlm.nih.gov/pubmed/24498619
http://dx.doi.org/10.1002/mgg3.30

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3865591/
https://www.ncbi.nlm.nih.gov/pubmed/24498619
http://dx.doi.org/10.1002/mgg3.30

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