reference/20613850

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endingPage	10554
issn	1091-6490 0027-8424
issueIdentifier	19
pageRange	10549-10554
publicationName	Proceedings of the National Academy of Sciences of the United States of America
startingPage	10549
bibliographicCitation	Zhang Y, Yasui N, Ito K, Huang G, Fujii M, Hanai J, Nogami H, Ochi T, Miyazono K, Ito Y. A RUNX2/PEBP2 αA/ CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia. Proc. Natl. Acad. Sci. U.S.A. 2000 Aug 29;97(19):10549–54. doi: 10.1073/pnas.180309597.
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date	2000-08-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1073/pnas.180309597 https://pubmed.ncbi.nlm.nih.gov/10962029 https://pubmed.ncbi.nlm.nih.gov/PMC27062
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A RUNX2/PEBP2 αA/ CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia
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