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Q58789077-00F1B03D-B41B-48D8-B36A-C8FB06E53FB5
Q58789077-00F1B03D-B41B-48D8-B36A-C8FB06E53FB5
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http://www.wikidata.org/entity/statement/Q58789077-00F1B03D-B41B-48D8-B36A-C8FB06E53FB5
Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review
P2860
Q58789077-00F1B03D-B41B-48D8-B36A-C8FB06E53FB5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58789077-00F1B03D-B41B-48D8-B36A-C8FB06E53FB5
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wasDerivedFrom
d26dd0932e782320426792d886c2b576b43fd0cb
P2860
Two domains unique to osteoblast-specific transcription factor Osf2/Cbfa1 contribute to its transactivation function and its inability to heterodimerize with Cbfbeta