Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.

Oral diseases - 1 Sept 2023

Yuan Minyan, Zheng Xueqing, Xue Yifan, He Zhenru, Song Guangtai, Song Yaling

Abstract excerpt

The present study aims to investigate the mutation in a Chinese family with dentin dysplasia type II (DD-II) and to summarize mutation hotspots, clinical manifestations, and disease management strategies. Phenotype analysis, clinical intervention, mutation screening, and cosegregation analysis within the enrolled family were performed. A summary of the reported mutations in the dentin phosphoprotein (DPP) region...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Dentin
Share to Dentinogenesis Imperfecta
Share to Disease Management

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Extracellular Matrix Proteins

Share to Frameshift Mutation

Share to Hyperplasia

Share to Nucleotides

Share to Sialoglycoproteins

Source

Identifiers

PMID: 36597617
DOI: 10.1111/odi.14494

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.PMID 36597617Read ↗

[Clinical and genetic analysis of a Chinese pedigree affected with Hereditary dentin dysplasia type II due to a variant of DSPP gene].Semantic proximity Read ↗

Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.Semantic proximity Read ↗

Identification of DSPP Novel Variants and Phenotype Analysis in dentinogenesis dysplasia shields type II PatientsSemantic proximity Read ↗

Withdrawal: A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.Semantic proximity Read ↗

Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients.Semantic proximity Read ↗

[Recognition on dentin dysplasia type Ⅱ].Semantic proximity Read ↗

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

Molecular basis of human dentin diseases.Semantic proximity Read ↗

Dentin dysplasia type I—A dental disease with genetic heterogeneitySemantic proximity Read ↗

[Clinical features and genetic mutation analysis of the hereditary dentin dysplasia type Ⅰ family].Semantic proximity Read ↗

Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II.Semantic proximity Read ↗

A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.