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Q41554454-BAD9B4FE-FE84-463C-B317-6E34D7031714
Q41554454-BAD9B4FE-FE84-463C-B317-6E34D7031714
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41554454-BAD9B4FE-FE84-463C-B317-6E34D7031714
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation.
P2860
Q41554454-BAD9B4FE-FE84-463C-B317-6E34D7031714
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41554454-BAD9B4FE-FE84-463C-B317-6E34D7031714
rank
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wasDerivedFrom
50748e454e4b880fcc46f5b657005a009718a765
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.