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Original research
Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy

Authors

  1. Correspondence to Dr Claude Cances, Neuropediatric Department, Toulouse University Hospital, Toulouse, France; cances.c{at}chu-toulouse.fr
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Citation

Géraud J, Dieterich K, Rendu J, et al
Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy

Publication history

  • Received November 15, 2019
  • Revised June 12, 2020
  • Accepted July 5, 2020
  • First published September 29, 2020.
Online issue publication 
August 20, 2021

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