A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A

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Hyperkalemic periodic paralysis and paramyotonia congenita caused by a de novo mutation in the SCN4A gene

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ژورنال

عنوان ژورنال: Neurology

سال: 2009

ISSN: 0028-3878,1526-632X

DOI: 10.1212/wnl.0b013e3181b87959