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Q28268653-033B173D-F4B8-4DD4-A119-0BA83CEF6B9E
Q28268653-033B173D-F4B8-4DD4-A119-0BA83CEF6B9E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28268653-033B173D-F4B8-4DD4-A119-0BA83CEF6B9E
Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy
P2860
Q28268653-033B173D-F4B8-4DD4-A119-0BA83CEF6B9E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28268653-033B173D-F4B8-4DD4-A119-0BA83CEF6B9E
rank
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wasDerivedFrom
f393fff88782222069900ab30490290cbf686f54
P2860
Rare copy number variants are an important cause of epileptic encephalopathies.