Mutational analysis of hemophilia B in Russia: Molecular-genetic study-Reference-Cited by-同舟云学术

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Mutational analysis of hemophilia B in Russia: Molecular-genetic study

Published:2016-04 Issue:4 Volume:52 Page:409-415
ISSN:1022-7954
Container-title:Russian Journal of Genetics
language:en
Short-container-title:Russ J Genet

Author:

Surin V. L.,Demidova E. Yu.,Selivanova D. S.,Luchinina Yu. A.,Salomashkina V. V.,Pshenichnikova O. S.,Likhacheva E. A.

Publisher

Pleiades Publishing Ltd

Subject

Genetics

Link

http://link.springer.com/content/pdf/10.1134/S1022795416040116.pdf

Reference29 articles.

1. Yoshitake, S., Schach, B.G., Foster, D.C., et al., Nucleotide sequence of the gene for human factor IX (antihemophilic factor B), Biochemistry, 1985, vol. 24, no. 14, pp. 3736–3750.

2. Ghosh, K., Quadros, L., and Shetty, S., Spectrum of factor IX gene mutations causing haemophilia B from India, Blood Coagulation Fibrinolysis, 2009, vol. 20, no. 5, pp. 333–336. doi 10.1097/MBC.0b013e32832b27d1

3. Elmahmoudi, H., Khodjet-El-Khil, H., Ben-Amor, M., et al., Identification of novel and recurrent mutations in Tunisian haemophilia B patients, Haemophilia, 2011, vol. 17, no. 3, pp. 544–545. doi 10.1111/j.13652516.2010.02442x

4. Awidi, A., Alhattab, D., Bsoul, N., et al., FIX mutation spectrum in haemophilia B patients from Jordan: identification of three novel mutations, Haemophilia, 2011, vol. 17, no. 1, pp. 162–163. doi 10.1111/j.13652516.2010.02365x

5. Halldén, C., Mårtensson, A., Nilsson, D., et al., Origin of Swedish hemophilia B mutations, J. Thromb. Haemostasis, 2013, vol. 11, no. 11, pp. 2001–2008. doi 10.1111/jth.12410

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1. Hemophilia B: Diagnosis and Management;Congenital Bleeding Disorders;2023

2. Hemophilia B Leyden: Literature and Our Data;Russian Journal of Genetics;2021-10

3. Defining the molecular pathology and consequent phenotypes in Egyptian HB patients;Journal of Genetic Engineering and Biotechnology;2021-05-17

4. Hemophilia B;Congenital Bleeding Disorders;2018

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