Published 2012 | Version v1.0.0
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POLG Novel Mutation with Alpers Syndrome

Abstract

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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PNB-2012-26-2-5

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Created
2012
When the item was originally created.