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Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene

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Footnotes

  • Funding This research was supported by a grant from the National Science Foundation of China (no 30470595).

  • Competing interests None.

  • Patient consent Obtained.

  • Ethics approval Ethics approval was obtained from the Bioethics Committee of Peking University First Hospital, Beijing, PR China.

  • Provenance and peer review Not commissioned; externally peer reviewed.