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Article

A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.

BMC medical genetics - 8 Aug 2007

Zhang Xianqin, Chen Lanying, Liu Jingyu, Zhao Zhen, Qu Erjun, Wang Xiaotao, Chang Wei, Xu Chengqi, Wang Qing K, Liu Mugen

Abstract excerpt

BACKGROUND: Hereditary defects of tooth dentin are classified into two main groups: dentin dysplasia (DD) (types I and II) and dentinogenesis imperfecta (DGI) (types I, II, and III). Type II DGI is one of the most common tooth defects with an autosomal dominant mode of inheritance. One disease-ca...

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Source

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Identifiers

PMID: 17686168
DOI: 10.1186/1471-2350-8-52
PMCID: PMC1995191

Genes

DSPP
DSP

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17686168-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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