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Q36809678-98D51B48-88FA-4F2A-923B-911F8B1EB906
Q36809678-98D51B48-88FA-4F2A-923B-911F8B1EB906
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Statement
http://www.wikidata.org/entity/statement/Q36809678-98D51B48-88FA-4F2A-923B-911F8B1EB906
14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
P2860
Q36809678-98D51B48-88FA-4F2A-923B-911F8B1EB906
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36809678-98D51B48-88FA-4F2A-923B-911F8B1EB906
rank
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wasDerivedFrom
fb4ac4a9bbc6c98804199e86d49768ff5f4e29fd
P2860
Regulation of protein kinase D1 activity.