| Literature DB >> 22565191 |
Hao Peng1, Yuhui Zhang, Zhigao Long, Ding Zhao, Zhenxin Guo, Jinjie Xue, Zhiguo Xie, Zhimin Xiong, Xiaojuan Xu, Wei Su, Bing Wang, Kun Xia, Zhengmao Hu.
Abstract
Osteogenesis imperfect (OI) is a heritable connective tissue disorder with bone fragility as a cardinal manifestation, accompanied by short stature, dentinogenesis imperfecta, hyperlaxity of ligaments and skin, blue sclerae and hearing loss. Dominant form of OI is caused by mutations in the type I procollagen genes, COL1A1/A2. Here we identified a novel splicing mutation c.3207+1G>A (GenBank ID: JQ236861) in the COL1A1 gene that caused type I OI in a Chinese family. RNA splicing analysis proved that this mutation created a new splicing site at c.3200, and then led to frameshift. This result further enriched the mutation spectrum of type I procollagen genes.Entities:
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Year: 2012 PMID: 22565191 DOI: 10.1016/j.gene.2012.04.023
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688