Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy.

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Title: Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy.
Authors: Poulton J (AUTHOR), Jayawant S (AUTHOR), O'Rourke A (AUTHOR), Morten K (AUTHOR), Ashley N (AUTHOR), Narasimhan M (AUTHOR), Fratter C (AUTHOR)
Source: Developmental Medicine & Child Neurology. Jan2007 Supplement 108, Vol. 49, p10-10. 1p.
Database: Academic Search Ultimate
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An: 105545655
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  Data: Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy.
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  Data: <searchLink fieldCode="JN" term="%22Developmental+Medicine+%26+Child+Neurology%22">Developmental Medicine & Child Neurology</searchLink>. Jan2007 Supplement 108, Vol. 49, p10-10. 1p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=105545655
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        Text: English
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      – TitleFull: Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy.
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              Text: Jan2007 Supplement 108
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              Y: 2007
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