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Novel ϵ subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome

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Footnotes

  • Competing interests: None.

  • Funding: Supported by AP-HP (PHRC AOM 01036), INSERM networks, GIS for Rare Diseases and the Association Française contre les Myopathies. DH was the recipient of an AP-HP interface contract.

  • Ethics approval: Ethics approval was provided by the local committee of CHRU of Lille.

  • Patient consent: Obtained.

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