A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia.

Source:http://linkedlifedata.com/resource/pubmed/id/10962029

Proc. Natl. Acad. Sci. U.S.A. 2000 Sep 12 97 19 10549-54

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PMID
10962029