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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| Natura: | Libro |
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Pediatric Neurology Briefs Publishers,
2012-02-01T00:00:00Z.
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A1234.567 |
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