Pediatric Neurology Briefs (Sep 2012)

Gene Identification in Alternating Hemiplegia

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-26-9-5
Journal volume & issue
Vol. 26, no. 9
pp. 69 – 69

Abstract

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Researchers at Georg Augustus University Gottingen, Germany studied the genetics of alternating hemiplegia of childhood (AHC) in 24 patients aged 8-35 years, using whole-exome sequencing to identify de novo mutations associated with the disease.

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