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Factor XIII Deficiency with a Novel Nonsense Mutation

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References

  1. Hsieh L, Nugent D (2008) Factor XIII deficiency. Haemophilia 14:1190–1200

    Article  CAS  PubMed  Google Scholar 

  2. Loewy AG, McDonagh J, Mikkola H, Teller DC, Yee VC (2001) Structure and function of factor XIII. In: Colmam RW, Hirsh J, Marder VJ, Clowes AW, George JN (eds) Hemostatis and thrombosis: basic principles and practice. Lippincott Williams and Wilkins, Philadelphia, pp 233–247

    Google Scholar 

  3. Sharma SK, Kumar S, Seth T, Mishra P et al (2012) Clinical profile of patients with rare inherited coagulation disorders: a retrospective analysis of 67 patients from Northern India. Mediterr J Hematol Infect Dis 4(1):e2012057

    Article  PubMed  PubMed Central  Google Scholar 

  4. Anwar R et al (2005) Factor XIII deficiency: new nonsense and deletion mutations in the human factor XIIIA gene. Haematologica 90(12):1718–1720

    CAS  PubMed  Google Scholar 

  5. Greenberg CS, Sane DC, Lai TS (2006) Factor XIII and fibrin stabilization. In: Colmam RW, Hirsh J, Marder VJ, George JN (eds) Hemostatis and thrombosis: basic principles and practice. Lippincott Williams and Wilkins, Philadelphia, pp 317–334

    Google Scholar 

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Authors and Affiliations

  1. Department of Hemato-Oncology and Bone Marrow Transplantation, BLK Superspeciality Hospital, New Delhi, 110005, India

    Vipin Khandelwal, Sanjeev Kumar Sharma, Divya Doval, Meet Kumar & Dharma Choudhary

  2. Department of Pediatric Critical Care, Center for Child Health, BLK Superspeciality Hospital, New Delhi, 110005, India

    Rachna Sharma

  3. MedGenome Labs Ltd, Bangalore, 560099, India

    Vedam L. Ramprasad

Authors
  1. Vipin Khandelwal
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  2. Sanjeev Kumar Sharma
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  3. Divya Doval
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  4. Meet Kumar
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  5. Dharma Choudhary
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  6. Rachna Sharma
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  7. Vedam L. Ramprasad
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Corresponding author

Correspondence to Vipin Khandelwal.

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The authors declare that they have no conflict of interest.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Informed consent was obtained from the patient’s parents in this study.

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Khandelwal, V., Sharma, S.K., Doval, D. et al. Factor XIII Deficiency with a Novel Nonsense Mutation. Indian J Hematol Blood Transfus 36, 588–589 (2020). https://doi.org/10.1007/s12288-020-01262-3

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  • DOI: https://doi.org/10.1007/s12288-020-01262-3

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