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Article

A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family.

BMC medical genetics - 10 Feb 2010

Bai Haihua, Agula Hasi, Wu Qizhu, Zhou Wenyu, Sun Yujing, Qi Yue, Latu Suya, Chen Yujie, Mutu Jiri, Qiu Changchun

Abstract excerpt

BACKGROUND: Several studies have shown that the clinical phenotypes of dentinogenesis imperfecta type II (DGI-II) may be caused by mutations in dentin sialophosphoprotein (DSPP). However, no previous studies have documented the clinical phenotype and genetic basis of DGI-II in a Mongolian family...

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Source

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Identifiers

PMID: 20146806
DOI: 10.1186/1471-2350-11-23
PMCID: PMC2829541

Genes

DSPP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-20146806-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family.PMID 20146806Read ↗

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[Clinical and genetic analysis of a pedigree affected with hereditary dentinogenesis imperfecta type II].Semantic proximity Read ↗

A novel splicing mutation alters DSPP transcription and leads to dentinogenesis imperfecta type II.Semantic proximity Read ↗

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