A Novel Gene Mutation of Runx2 in Cleidocranial Dysplasia

Haploinsufficiency of the runt-related transcription factor 2（Runx2） gene is widely known to be responsible for cleidocranial dysplasia（CCD）. To date, more than 190 mutations in Runx2 gene have been reported to be related to CCD. In this study, a novel mutation of Runx2 gene was observed in a female...

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Bibliographic Details

Published in:	Current medical science Vol. 37; no. 5; pp. 772 - 776
Main Author:	彭友俭;陈巧云;付东杰;刘志明;毛甜甜;李俊;佘文婷
Format:	Journal Article
Language:	English
Published:	Wuhan Huazhong University of Science and Technology 01-10-2017 Department of Stomatology, Renmin Hospital of Wuhan University, Wuhan 430060, China
Subjects:	Medicine Medicine & Public Health mutation genetic testing RUNX2 cleidocranial dysplasia
Online Access:	Get full text
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