从血友病B Leyden的恢复:因子IX促进器中的一个雄激素反应元素
M Crossley1, M Ludwig, K M Stowell
1Chemical Pathology Unit, Sir William Dunn School of Pathology, University of Oxford, United Kingdom.
概括
血友性B,一种遗传性出血障碍,由于特定的基因突变,在青春期后得到改善. 这些突变影响了凝血因子IX基因转录,其中一个突变也影响了对雄激素敏感的元素.
科学领域:
- 遗传学和分子生物学
- 血液学 血液学 血液学
- 内分泌学 在内分泌学.
背景情况:
- 血友性B是一种X系遗传性出血障碍.
- 这种情况通常在青春期后会有所改善.
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