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The VEXAS syndrome from rheumatology perspective: genomic DNA sequencing as available blueprint for diagnosing rheumatic diseases with overlap** haematological or dermatological findings

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References

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Authors and Affiliations

  1. Department of Rheumatology and Medicine, Southport and Ormskirk NHS Trust, Southport, PR8 6PN, UK

    Arvind Nune

  2. Department of Trauma and Orthopaedics, Southport and Ormskirk Hospital NHS Trust, Southport, PR8 6PN, UK

    Karthikeyan P. Iyengar

  3. Department of Medicine, North Eastern Indira Gandhi Regional Institute of Health and Medical Sciences, NEIGRIHMS0, Shillong, Meghalaya, India

    Bhupen Barman

  4. Department of Rheumatology, Rheumatologic Outpatient Clinic, “Mariano Lauro” Hospital, Azienda Sanitaria Locale Napoli 3 Sud, Sant’Agnello, Campania, Italy

    Ciro Manzo

Authors
  1. Arvind Nune
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  2. Karthikeyan P. Iyengar
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  3. Bhupen Barman
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  4. Ciro Manzo
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Contributions

AN conceptualised and written initial draft. KPI, BB and CM involved in data curation, writing review and editing. All authors read, validated and authorised the final version of the manuscript.

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Correspondence to Arvind Nune.

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Nune, A., Iyengar, K.P., Barman, B. et al. The VEXAS syndrome from rheumatology perspective: genomic DNA sequencing as available blueprint for diagnosing rheumatic diseases with overlap** haematological or dermatological findings. Clin Rheumatol 41, 2917–2918 (2022). https://doi.org/10.1007/s10067-022-06211-1

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  • DOI: https://doi.org/10.1007/s10067-022-06211-1

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