POLG Novel Mutation with Alpers Syndrome
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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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2012-02-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/574 |