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Updated: Jul 13, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family

Xianqin Zhang1, Lanying Chen, Jingyu Liu

  • 1Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology and Center for Human Genome Research, Huazhong University of Science and Technology, Wuhan, Hubei 430074, China. zhangx3@ccf.org

BMC Medical Genetics
|August 10, 2007
PubMed
Abstract

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