Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency
Author:
Funder
Department of Biotechnology, Ministry of Science and Technology, India
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12288-022-01579-1.pdf
Reference20 articles.
1. Alshehri FSM, Whyte CS, Mutch NJ (2021) Factor XIII-A: An Indispensable “Factor” in Haemostasis and Wound Healing. Int J Mol Sci 22:3055
2. Karimi M, Bereczky Z, Cohan N, Muszbek L (2009) Factor XIII Deficiency. Semin Thromb Hemost 35:426–438
3. Kohler HP, Ichinose A, Seitz R et al (2011) Diagnosis and classification of factor XIII deficiencies. J Thromb Haemost 9:1404–1406
4. Muszbek L, Katona É (2016) Diagnosis and Management of Congenital and Acquired FXIII Deficiencies. Semin Thromb Hemost 42:429–439
5. Anwar R, Stewart AD, Miloszewski KJA et al (1995) Molecular basis of inherited factor XIII deficiency: identification of multiple mutations provides insights into protein function. Br J Haematol 91:728–735
Cited by 2 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. Correction to: Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency;Indian Journal of Hematology and Blood Transfusion;2023-03-06
2. Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect;Haemophilia;2022-12-26
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