Pediatric Neurology Briefs (Feb 2012)

POLG Novel Mutation with Alpers Syndrome

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-26-2-5
Journal volume & issue
Vol. 26, no. 2
pp. 12 – 12

Abstract

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Researchers at University Hospital, Berne, Switzerland describe the molecular genetic analysis of POLG in a 3.5 years old boy with VPA-induced fatal liver failure and encephalopathy (Alpers-Huttenlocher syndrome, AHS).

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