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Q37132419-0AE1BAFB-235D-4178-BBC2-E7F089D4B5EF
Q37132419-0AE1BAFB-235D-4178-BBC2-E7F089D4B5EF
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Statement
http://www.wikidata.org/entity/statement/Q37132419-0AE1BAFB-235D-4178-BBC2-E7F089D4B5EF
Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.
P2860
Q37132419-0AE1BAFB-235D-4178-BBC2-E7F089D4B5EF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132419-0AE1BAFB-235D-4178-BBC2-E7F089D4B5EF
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wasDerivedFrom
f1dbaa5b6e36ebc75f4356b465e56c996004f3e2
P2860
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases.