De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
17:50 EDT 29 Jul 2012 | Nature Publishing
David Goldstein, Mohamad Mikati and colleagues report identification of de novo mutations in ATP1A3 in alternating hemiplegia of childhood, which is a rare neurodevelopmental syndrome characterized by recurrent hemiplegic episodes and distinct neurol..
Original Article: De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
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