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Case report
Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure

Authors

  1. Correspondence to Dr Patel Zeeshan Jameel; zeeshan1311{at}gmail.com
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Citation

Kinkar JS, Jameel PZ, Kumawat BL, et al
Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure
BMJ Case Reports CP 2021;14:e241767.

Publication history

  • Accepted May 29, 2021
  • First published June 30, 2021.
Online issue publication 
January 24, 2024

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© BMJ Publishing Group Limited 2021. No commercial re-use. See rights and permissions. Published by BMJ.