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Q37132419-5F7CB799-7812-4D18-9626-8CBC64A456E4
Q37132419-5F7CB799-7812-4D18-9626-8CBC64A456E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132419-5F7CB799-7812-4D18-9626-8CBC64A456E4
Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.
P2860
Q37132419-5F7CB799-7812-4D18-9626-8CBC64A456E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132419-5F7CB799-7812-4D18-9626-8CBC64A456E4
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wasDerivedFrom
c2785608bd2fc7b709b468f1506485d40cee722d
P2860
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion.