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Q50744408-5095EB36-5525-4BC9-B2A8-0DAF4021F68F
Q50744408-5095EB36-5525-4BC9-B2A8-0DAF4021F68F
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Statement
http://www.wikidata.org/entity/statement/Q50744408-5095EB36-5525-4BC9-B2A8-0DAF4021F68F
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR.
P2860
Q50744408-5095EB36-5525-4BC9-B2A8-0DAF4021F68F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50744408-5095EB36-5525-4BC9-B2A8-0DAF4021F68F
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wasDerivedFrom
d4165cd9d4ec865a09b287a7a7128be230d5e881
P2860
Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females.