Article Text
PostScript
Letter
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.