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Defects of splicing in antithrombin deficiency
ESSENTIALS: Increasing evidences supports a role for splicing defects in multiple disorders. For antithrombin (AT) deficiency only 7% of mutations disturb intronic splicing sequences. Our study of 141 unrelated cases with AT deficiency found higher rate of splicing defects (>13%). A wide range of...
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| 發表在: | Res Pract Thromb Haemost |
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| Main Authors: | , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6058262/ https://ncbi.nlm.nih.gov/pubmed/30046692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/rth2.12025 |
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