THE IDENTIFICATION OF HAEMOPHILIA B MUTATIONS
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Publisher
Elsevier
Reference21 articles.
1. The gene structure of human anti-haemophilic factor IX.
2. Defective propeptide processing of blood clotting factor IX caused by mutation of arginine to glutamine at position −4
3. Assignment of the haemophilia B (Factor IX) locus to the q26-qter region of the X chromosome
4. The Molecular Genetics of Haemophilia A and B
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A new strategy for the genetic counselling of diseases of marked mutational heterogeneity: haemophilia B as a model.;Journal of Medical Genetics;1992-09-01
2. Genomische Diagnostik und Charakterisierung molekularer Defekte bei Hämophilie B;22. Hämophilie-Symposion Hamburg 1991;1992
3. Haemophilia B mutations in a complete Swedish population sample: a test of new strategy for the genetic counselling of diseases with high mutational heterogeneity;British Journal of Haematology;1991-07
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