A genetic analysis of 23 Chinese patients with hemophilia B

Hemophilia B (HB) is an X-linked recessive bleeding disorder caused by mutations in the coagulation factor IX (FIX) gene. Genotyping patients with HB is essential for genetic counseling and provides useful information for patient management. In this study, the F9 gene from 23 patients with HB was an...

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Detalles Bibliográficos
Autores principales: Wang, Qing-Yun, Hu, Bei, Liu, Hui, Tang, Liang, Zeng, Wei, Wu, Ying-Ying, Cheng, Zhi-Peng, Hu, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842959/
https://www.ncbi.nlm.nih.gov/pubmed/27109384
http://dx.doi.org/10.1038/srep25024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842959/
https://www.ncbi.nlm.nih.gov/pubmed/27109384
http://dx.doi.org/10.1038/srep25024

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