Enamel-renal-gingival syndrome andFAM20Amutations-Reference-Cited by-同舟云学术

Enamel-renal-gingival syndrome andFAM20Amutations

Published:2013-11-20 Issue:1 Volume:164 Page:1-9
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kantaputra Piranit Nik¹²³,Kaewgahya Massupa²,Khemaleelakul Udomrat⁴,Dejkhamron Prapai⁵,Sutthimethakorn Suchitra⁶,Thongboonkerd Visith⁶,Iamaroon Anak⁷

Affiliation:

1. Division of Pediatric Dentistry; Department of Orthodontics and Pediatric Dentistry, Chiang Mai University; Chiang Mai Thailand

2. Craniofacial Genetics Laboratory; Faculty of Dentistry, Chiang Mai University; Chiang Mai Thailand

3. DENTALAND CLINIC; Chiang Mai Thailand

4. Department of Oral and Maxillofacial Surgery; Faculty of Dentistry, Chiang Mai University; Chiang Mai Thailand

5. Department of Pediatrics; Faculty of Medicine; Chiang Mai University; Chiang Mai Thailand

6. Medical Proteomics Unit and Center for Research in Complex Systems Science; Faculty of Medicine Siriraj Hospital, Mahidol University; Bangkok Thailand

7. Department of Oral Biology and Diagnostic Science; Faculty of Dentistry, Chiang Mai University; Chiang Mai Thailand

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference41 articles.

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2. Amelogenesis imperfecta with gingival calcification: A rare presentation;Carnelio;Braz J Oral Sci,2005

3. Raine syndrome: A rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings;Chitayat;Am J Med Genet Part A,2007

4. Novel FAM20A mutations in hypoplastic amelogenesis imperfecta;Cho;Hum Mutat,2011

5. Hyperparathyroidism: Primary or secondary disease;Cordellat;Reumatol Clin,2012

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1. Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosis;Scientific Reports;2024-04-25

2. Dental and jawbone abnormalities linked to amelogenesis imperfecta: A retrospective and analytic study comparing panoramic radiographs;Special Care in Dentistry;2023-10-26

3. Epithelial-specific deletion of FAM20A leads to short root defects;Gene;2023-10

4. Enamel renal syndrome: A case report with calcifications in pulp, gingivae, dental follicle and kidneys;Special Care in Dentistry;2023-08-09

5. Potential Role of Protein Kinase FAM20C on the Brain in Raine Syndrome, an In Silico Analysis;International Journal of Molecular Sciences;2023-05-17