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Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent

Authors

  1. Correspondence to Dr Eunice Sindhuvi Edison, Department of Haematology, Christian Medical College, Vellore 632004, Tamil Nadu, India; eunice{at}cmcvellore.ac.in
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Citation

Ravindra N, Athiyarath R, S E, et al
Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent

Publication history

  • Received April 11, 2020
  • Revised June 3, 2020
  • Accepted June 5, 2020
  • First published June 30, 2020.
Online issue publication 
February 18, 2021

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