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POLG mutations and Alpers syndrome

Published:2005 Issue:6 Volume:57 Page:921-923
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Davidzon Guido,Mancuso Michelangelo,Ferraris Silvio,Quinzii Catarina,Hirano Michio,Peters Heidi L.,Kirby Denise,Thorburn David R.,DiMauro Salvatore

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference20 articles.

1. DIFFUSE PROGRESSIVE DEGENERATION OF THE GRAY MATTER OF THE CEREBRUM

2. Infantile Diffuse Cerebral Degeneration With Hepatic Cirrhosis

3. Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity

4. The incidence of mitochondrial encephalomyopathies in childhood: Clinical features and morphological, biochemical, and DNA abnormalities

5. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion

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