Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta-Reference-Cited by-同舟云学术

Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta

Published:2018-08-17 Issue:3 Volume:23 Page:1481-1487
ISSN:1432-6981
Container-title:Clinical Oral Investigations
language:en
Short-container-title:Clin Oral Invest

Author:

Kim Youn Jung,Seymen Figen,Kang Jenny,Koruyucu Mine,Tuloglu Nuray,Bayrak Sule,Tuna Elif Bahar,Lee Zang Hee,Shin Teo Jeon,Hyun Hong-Keun,Kim Young-Jae,Lee Sang-Hoon,Hu Jan,Simmer James,Kim Jung-Wook^ORCID

Funder

National Research Foundation of Korea

National Institute of Dental and Craniofacial Research

Publisher

Springer Science and Business Media LLC

Subject

General Dentistry

Link

http://link.springer.com/content/pdf/10.1007/s00784-018-2577-9.pdf

Reference36 articles.

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3. Witkop CJ Jr (1988) Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification. J Oral Pathol 17:547–553. https://doi.org/10.1111/j.1600-0714.1988.tb01332.x

4. Lagerstrom M, Dahl N, Nakahori Y, Nakagome Y, Backman B, Landegren U, Pettersson U (1991) A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1). Genomics 10:971–975. https://doi.org/10.1016/0888-7543(91)90187-j

5. Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ (2001) Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta. Hum Mol Genet 10:1673–1677. https://doi.org/10.1093/hmg/10.16.1673

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