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Q34177297-E57B7C47-6BE3-4D12-8253-2AA786C6EC8F
Q34177297-E57B7C47-6BE3-4D12-8253-2AA786C6EC8F
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Statement
http://www.wikidata.org/entity/statement/Q34177297-E57B7C47-6BE3-4D12-8253-2AA786C6EC8F
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.
P2860
Q34177297-E57B7C47-6BE3-4D12-8253-2AA786C6EC8F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34177297-E57B7C47-6BE3-4D12-8253-2AA786C6EC8F
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wasDerivedFrom
afbe6743226cf710a4aaec0fdebde30596c920ac
P2860
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.