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Mutation analysis in the F8 gene in 485 families with haemophilia A and prenatal diagnosis in China
BACKGROUND: Haemophilia A (HA) is an X‐linked bleeding disorder caused by mutations in the coagulation factor Ⅷ (F8) gene. Its incidence in men is estimated to be approximately 1/5000. OBJECTIVE: This study aimed to characterize the mutation spectrum of the F8 gene in 485 Chinese families, encompass...
Sparad:
| I publikationen: | Haemophilia |
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| Huvudupphovsmän: | , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
John Wiley and Sons Inc.
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7898705/ https://ncbi.nlm.nih.gov/pubmed/33245802 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/hae.14206 |
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