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Q37317012-64C99F24-FC83-41EC-8EA0-EF73BAB9C30C
Q37317012-64C99F24-FC83-41EC-8EA0-EF73BAB9C30C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37317012-64C99F24-FC83-41EC-8EA0-EF73BAB9C30C
Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.
P2860
Q37317012-64C99F24-FC83-41EC-8EA0-EF73BAB9C30C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37317012-64C99F24-FC83-41EC-8EA0-EF73BAB9C30C
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Statement
wasDerivedFrom
16421847425f56fb8e70bdf9a19e425c93e16cc4
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.