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Q34576300-23D15D03-6B76-4769-BC88-5FFD9E97B3B9
Q34576300-23D15D03-6B76-4769-BC88-5FFD9E97B3B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34576300-23D15D03-6B76-4769-BC88-5FFD9E97B3B9
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.
P2860
Q34576300-23D15D03-6B76-4769-BC88-5FFD9E97B3B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34576300-23D15D03-6B76-4769-BC88-5FFD9E97B3B9
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Statement
wasDerivedFrom
70957a1c40267fa60a27ed016a03f62e3d841f7c
P2860
Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature.