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A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia
Author(s):
YW Zhang
,
N Yasui
,
K. Ito
,
G Huang
,
M Fujii
,
J Hanai
,
H. Nogami
,
T. Ochi
,
K Miyazono
,
Y Ito
Publication date:
2000
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Molecular biology
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Genetics
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Life sciences
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