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Q34482877-EE32B21D-958F-42A7-A553-38379FC96EFD
Q34482877-EE32B21D-958F-42A7-A553-38379FC96EFD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34482877-EE32B21D-958F-42A7-A553-38379FC96EFD
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.
P2860
Q34482877-EE32B21D-958F-42A7-A553-38379FC96EFD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34482877-EE32B21D-958F-42A7-A553-38379FC96EFD
rank
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Statement
wasDerivedFrom
1dbd40c6334ef01a48fdfadc4ce9118864593a47
P2860
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.