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  • RNA sequencing uncovers clinically actionable germline intronic MSH2 variants in previously unresolved Lynch syndrome families

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Case Reports: Novel diagnostic procedure
RNA sequencing uncovers clinically actionable germline intronic MSH2 variants in previously unresolved Lynch syndrome families

Authors

  1. Correspondence to Kelly Fulk; kfulk{at}ambrygen.com
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Citation

Fulk K, Turner M, Eppolito A, et al
RNA sequencing uncovers clinically actionable germline intronic MSH2 variants in previously unresolved Lynch syndrome families
BMJ Case Reports CP 2022;15:e249580.

Publication history

  • Accepted April 12, 2022
  • First published April 29, 2022.
Online issue publication 
January 24, 2024

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© BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.