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Q37132419-2BD3F797-9F51-4419-AE34-613F7BE3B173
Q37132419-2BD3F797-9F51-4419-AE34-613F7BE3B173
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132419-2BD3F797-9F51-4419-AE34-613F7BE3B173
Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.
P2860
Q37132419-2BD3F797-9F51-4419-AE34-613F7BE3B173
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132419-2BD3F797-9F51-4419-AE34-613F7BE3B173
rank
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type
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Statement
wasDerivedFrom
f1dbaa5b6e36ebc75f4356b465e56c996004f3e2
P2860
Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.