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Recuperación de la hemofilia B Leyden: un elemento sensible a los andrógenos en el promotor del factor IX
M Crossley1, M Ludwig, K M Stowell
1Chemical Pathology Unit, Sir William Dunn School of Pathology, University of Oxford, United Kingdom.
La hemofilia B, un trastorno hemorrágico hereditario, mejora después de la pubertad debido a mutaciones genéticas específicas. Estas mutaciones afectan a la transcripción del gen del factor de coagulación IX, con una mutación que también afecta a un elemento sensible a los andrógenos.
Área de la Ciencia:
- Genética y Biología Molecular.
- Hematología Hematología.
- Endocrinología Endocrinología.
Sus antecedentes:
- La hemofilia B es un trastorno hemorrágico hereditario vinculado a X.
- La condición a menudo muestra mejoría después de la pubertad.
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