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Gene Identification in Alternating Hemiplegia Cover

Gene Identification in Alternating Hemiplegia

Open Access
|Sep 2012

References

  1. Rosewich H Thiele H Ohlenbusch A Maschke U Altmüller J Frommolt P Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study Lancet Neurol 2012 Sep 11 9 764 73 10.1016/S1474-4422(12)70182-5 22850527
  2. Heinzen EL Swoboda KJ Hitomi Y Gurrieri F Nicole S de Vries B De novo mutations in ATP1A3 cause alternating hemiplegia of childhood Nat Genet 2012 Sep 44 9 1030 4 10.1038/ng.2358 22842232
  3. Saito Y Inui T Sakakibara T Sugai K Sakuma H Sasaki M Evolution of hemiplegic attacks and epileptic seizures in alternating hemiplegia of childhood Epilepsy Res 2010 Aug 90 3 248 58 10.1016/j.eplepsyres.2010.05.013 20580529
Language: English
Page range: 69 - 69
Published on: Sep 1, 2012
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services

© 2012 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.