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Q37172192-51039B89-D5F0-45A8-93AD-18AA0B869A32
Q37172192-51039B89-D5F0-45A8-93AD-18AA0B869A32
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37172192-51039B89-D5F0-45A8-93AD-18AA0B869A32
MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways.
P2860
Q37172192-51039B89-D5F0-45A8-93AD-18AA0B869A32
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37172192-51039B89-D5F0-45A8-93AD-18AA0B869A32
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type
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wasDerivedFrom
7218a49fffcdcb56e4cb833f444803f2461f21d6
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.