Compound Heterozygous Polymerase Gamma Gene Mutation in a Patient With Alpers Disease
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Reference19 articles.
1. Diffuse progressive degeneration of gray matter of cerebrum;Alpers;Arch Neurol,1931
2. Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): A personal review;Harding;J Child Neurol,1990
3. Infantile diffuse cerebral degeneration with hepatic cirrhosis;Huttenlocher;Arch Neurol,1976
4. Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults;Harding;J Neurol Neurosurg Psychiatry,1995
5. Homozygous W74 8S mutation in the POLG1 gene in patients with juvenile-onset Alpers' syndrome and status epilepticus;Uusimaa;Epilepsia,2008
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