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Gray Platelet Syndrome with Severe Thrombocytopenia: A Novel NBEAL2 Gene Variant from India

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Patient data is available on request from corresponding author.

References

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Acknowledgements

The authors extend their sincere thanks to Dr. Michele P. Lambert, Medical Director ­ Special Coagulation Laboratory, Associate Professor ­ Department of Pediatrics, Attending Physician—Division of Hematology Children's Hospital of Philadelphia, USA for sharing her expertise.

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None to declare.

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Authors and Affiliations

  1. Division of Pediatric Hematology and Oncology, Manipal Comprehensive Cancer Care Centre, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India

    Archana Mevalegire Venkatagiri, Kalasekhar Vijayasekharan & K. Vasudeva Bhat

  2. Department of Pathology, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, Karnataka, 576104, India

    Sindhura Lakshmi Koulmane Laxminarayana, Sushma Belurkar & Vishwapriya Mahadev Godkhindi

Authors
  1. Archana Mevalegire Venkatagiri
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  2. Kalasekhar Vijayasekharan
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  3. K. Vasudeva Bhat
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  4. Sindhura Lakshmi Koulmane Laxminarayana
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  5. Sushma Belurkar
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  6. Vishwapriya Mahadev Godkhindi
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Contributions

VMG: Conceptualization, Methodology, Formal analysis, Investigation, Manuscript editing and Manuscript review. AMV: Methodology, Literature search, Investigation, Manuscript preparation and Manuscript review. KV: Methodology, Manuscript preparation, Formal analysis, Manuscript editing and Manuscript review. VBK, SLKL, SB: Methodology, Formal analysis, Manuscript editing and Manuscript review.

Corresponding author

Correspondence to Vishwapriya Mahadev Godkhindi.

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In accordance with ethical standards of the institutional ethics committee & with the 1964 Helsinki declaration and its later amendments or comparable national/international guidelines.

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Written informed consent was obtained from all the participants in the study.

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Mevalegire Venkatagiri, A., Vijayasekharan, K., Bhat, K.V. et al. Gray Platelet Syndrome with Severe Thrombocytopenia: A Novel NBEAL2 Gene Variant from India. Indian J Hematol Blood Transfus 38, 754–756 (2022). https://doi.org/10.1007/s12288-022-01531-3

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  • DOI: https://doi.org/10.1007/s12288-022-01531-3

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