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Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations
BACKGROUND: Hemophilia B (HB) is an X‐linked recessive inherited bleeding disorder caused by mutations in the F9 gene that lead to plasma factor IX deficiency. To identify the causative mutations in HB, a molecular analysis of HB pedigrees in China was performed. METHODS: Using next‐generation seque...
Shranjeno v:
| izdano v: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
John Wiley and Sons Inc.
2020
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7667291/ https://ncbi.nlm.nih.gov/pubmed/32875744 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1482 |
| Oznake: |
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