Two rare variants reveal the significance of Grainyhead‐like 3 Arginine 391 underlying non‐syndromic cleft palate only-Reference-Cited by-同舟云学术

Two rare variants reveal the significance of Grainyhead‐like 3 Arginine 391 underlying non‐syndromic cleft palate only

Published:2022-04-19 Issue:4 Volume:29 Page:1632-1643
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:Oral Diseases

Author:

Huang Wenbin¹²^ORCID,He Qing³,Li Mingzhao¹²,Ding Yi³,Liang Wei¹²,Li Weiran¹²,Lin Jiuxiang¹²,Zhao Huaxiang⁴⁵^ORCID,Chen Feng²⁶^ORCID

Affiliation:

1. Department of Orthodontics Peking University School and Hospital of Stomatology Beijing China

2. National Center of Stomatology National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory for Digital Stomatology, Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health, NMPA Key Laboratory for Dental Materials Beijing China

3. Department of Physiology and Pathophysiology School of Basic Medical Sciences Xi’an Jiaotong University Health Science Center Xi’an China

4. Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research College of Stomatology Xi’an Jiaotong University Xi'an China

5. Department of Orthodontics College of Stomatology Xi’an Jiaotong University Xi’an China

6. Central Laboratory Peking University School and Hospital of Stomatology Beijing China

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/odi.14164

Reference52 articles.

1. A method and server for predicting damaging missense mutations

2. Periderm Cells Form Cornified Cell Envelope in Their Regression Process During Human Epidermal Development

3. Spatial and temporal expression of the Grainyhead-like transcription factor family during murine development

4. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes

5. Genomic analyses in African populations identify novel risk loci for cleft palate

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