Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia

Author:

Zeng Li,Wei Jiahui,Han Dong,Liu Haochen,Liu Yang,Zhao Na,Sun Shichen,Wang Yixiang,Feng Hailan

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Genetics (clinical),Toxicology,Genetics

Reference26 articles.

1. Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia;Am. J. Hum. Genet.,1999

2. Histological observations of teeth and peridental tissues in cleidocranial dysplasia imply increased activity of odontogenic epithelium and abnormal bone remodeling;J. Craniofac. Genet. Dev. Biol.,1995

3. Restorative treatment strategies for patients with cleidocranial dysplasia;Acta Odontol. Scand.,2015

4. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia;Nat. Genet.,1997

5. Cleidocranial dysplasia: clinical and molecular genetics;J. Med. Genet.,1999

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