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Q38500985-2C50538A-6A5B-4354-9BAB-CF8C2BC52A9F
Q38500985-2C50538A-6A5B-4354-9BAB-CF8C2BC52A9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38500985-2C50538A-6A5B-4354-9BAB-CF8C2BC52A9F
High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations.
P2860
Q38500985-2C50538A-6A5B-4354-9BAB-CF8C2BC52A9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38500985-2C50538A-6A5B-4354-9BAB-CF8C2BC52A9F
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Statement
wasDerivedFrom
e7fed9a83211b713a627f4e24c55fdffd2fdba00
P2860
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.