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Mutation analysis of a cohort of US patients with hemophilia B

Hemophilia B (HB) is a disorder resulting from genetic mutations in the Factor 9 gene (F9). Genotyping of HB patients is important for genetic counseling and patient management. Here we report a study of mutations identified in a large sample of HB patients in the US. Patients were enrolled through...

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Detalhes bibliográficos
Publicado no:Am J Hematol
Main Authors: Li, Tengguo, Miller, Connie H., Driggers, Jennifer, Payne, Amanda B., Ellingsen, Dorothy, Hooper, W. Craig
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4504203/
https://ncbi.nlm.nih.gov/pubmed/24375831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.23645
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