Novel frameshift mutations in DSPP cause dentin dysplasia type II-Reference-Cited by-同舟云学术

Novel frameshift mutations in DSPP cause dentin dysplasia type II

Published:2019-09-11 Issue:8 Volume:25 Page:2044-2046
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:Oral Dis

Author:

Lee Ji Won¹,Hong Jiwon¹,Seymen Figen²,Kim Youn Jung³,Kang Jenny¹,Koruyucu Mine²,Tuloglu Nuray⁴,Bayrak Sule⁴,Song Ji‐Soo¹,Shin Teo Jeon¹,Hyun Hong‐Keun¹,Kim Young‐Jae¹,Lee Jae‐Cheoun⁵,Park Joo‐Cheol⁶,Hu Jan⁷,Simmer James⁷,Kim Jung‐Wook¹³^ORCID

Affiliation:

1. Department of Pediatric Dentistry & Dental Research Institute School of Dentistry Seoul National University Seoul Korea

2. Department of Pedodontics Faculty of Dentistry Istanbul University Istanbul Turkey

3. Department of Molecular Genetics & Dental Research Institute School of Dentistry Seoul National University Seoul Korea

4. Department of Pediatric Dentistry Faculty of Dentistry University of Eskisehir Osmangazi Eskisehir Turkey

5. Seoul Chungdam Children's Dental Center Seoul Korea

6. Department of Cell and Developmental Biology & Dental Research Institute School of Dentistry Seoul National University Seoul Korea

7. Department of Biologic and Materials Sciences School of Dentistry University of Michigan Ann Arbor MI USA

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/odi.13182

Reference10 articles.

1. Phenotypic Variation in Dentinogenesis Imperfecta/Dentin Dysplasia Linked to 4q21

2. Evolutionary genetics of vertebrate tissue mineralization: the origin and evolution of the secretory calcium-binding phosphoprotein family

3. Hereditary Dentin Defects

4. Overlapping DSPP Mutations Cause Dentin Dysplasia and Dentinogenesis Imperfecta

5. A comprehensive analysis of normal variation and disease-causing mutations in the humanDSPPgene

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2. The Quebec Dental Anomalies Registry: Identifying genes for rare disorders;PNAS Nexus;2023-05-31

3. Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients;Clinical Oral Investigations;2023-04-05

4. A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies;Oral Diseases;2023-01-13

5. The Modified Shields Classification and 12 Families with Defined DSPP Mutations;Genes;2022-05-12