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Q38429148-9D8F8877-E145-40C1-B10C-152A4C2FFA22
Q38429148-9D8F8877-E145-40C1-B10C-152A4C2FFA22
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Statement
http://www.wikidata.org/entity/statement/Q38429148-9D8F8877-E145-40C1-B10C-152A4C2FFA22
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus.
P2860
Q38429148-9D8F8877-E145-40C1-B10C-152A4C2FFA22
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38429148-9D8F8877-E145-40C1-B10C-152A4C2FFA22
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wasDerivedFrom
5f9ae220c95fc59c33742fc23a708430f297e173
P2860
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome