A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia (Q24652629)
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Current Data About A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia
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(P1476) "A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia" (language: en)

(P2093) Y W Zhang
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N Yasui
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K Ito
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G Huang
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M Fujii
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J Hanai
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H Nogami
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T Ochi
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K Miyazono
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Y Ito
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