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Q34482877-265B1C41-532E-489F-9B99-8A67451639AE
Q34482877-265B1C41-532E-489F-9B99-8A67451639AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34482877-265B1C41-532E-489F-9B99-8A67451639AE
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.
P2860
Q34482877-265B1C41-532E-489F-9B99-8A67451639AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34482877-265B1C41-532E-489F-9B99-8A67451639AE
rank
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type
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Statement
wasDerivedFrom
1dbd40c6334ef01a48fdfadc4ce9118864593a47
P2860
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation