Published 2012
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POLG Novel Mutation with Alpers Syndrome
- Creators
- Millichap, J. Gordon
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.pdf
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- PNB-2012-26-2-5
- Created
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2012When the item was originally created.