Cargando…
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...
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: | |
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 |
Ejemplares similares
-
APOC3 may not be a predictor of risk of ischemic vascular disease in the Chinese population
por: Tang, Liang, et al.
Publicado: (2014) -
Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice
por: Pezeshkpoor, Behnaz, et al.
Publicado: (2022) -
Clinical and genetic characteristics of Chinese patients with cerebrotendinous xanthomatosis
por: Tao, Qing-Qing, et al.
Publicado: (2019) -
The Clinical Genetics of Hemophilia B (Factor IX Deficiency)
por: Miller, Connie H
Publicado: (2021) -
Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population
por: Wu, Yingying, et al.
Publicado: (2022)