Skip to main content

Advertisement

Log in

Somatic Hemizygous Y371H CBL Mutation with Loss of Heterozygosity Presenting with BENTA Type Lymphoid Proliferation

  • Images
  • Published:
Indian Journal of Hematology and Blood Transfusion Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

References

  1. Pérez B, Mechinaud F, Galambrun C, Ben Romdhane N, Isidor B, Philip N et al (2010) Germline mutations of the CBL gene define a new genetic syndrome with predisposition to juvenile myelomonocytic leukaemia. J Med Genet 47(10):686

    Article  PubMed  Google Scholar 

  2. Brohl AS, Stinson J, Su HC, Badgett T, Jennings CD, Sukumar G et al (2015) Germline CARD11 mutation in a patient with severe congenital B cell lymphocytosis. J Clin Immunol 35(1):32–46

    Article  PubMed  Google Scholar 

Download references

Funding

No funding received.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Narender Tejwani.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Disclaimer The identity of the patient is not disclosed here in this case.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tejwani, N., Tayal, P., Mehta, A. et al. Somatic Hemizygous Y371H CBL Mutation with Loss of Heterozygosity Presenting with BENTA Type Lymphoid Proliferation. Indian J Hematol Blood Transfus 36, 594–596 (2020). https://doi.org/10.1007/s12288-019-01243-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12288-019-01243-1

Navigation