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"Dentin bonding strength of packable composites using one-bottle adhesives

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Authors
Kim, Jung-Wook; Lee, Sook-Kyung; Lee, Zang Hee; Park, Joo-Cheol; Lee, Kyung-Eun; Lee, Myoung-Hwa; Park, Jong-Tae; Seo, Byoung-Moo; Hu, Jan C.-C.; Simmer, James P.
Issue Date
2008
Publisher
MOSHER AND LINDER
Citation
AMERICAN JOURNAL OF HUMAN GENETICS 82, 489-494, 2008
Abstract
Amelogenesis imperfecta (AI) is a collection of diverse inherited disorders featuring dental-enamel defects in the absence of significant nondental symptoms. AI phenotypes vary and are categorized as hypoplastic, hypocalcified, and hypomaturation types. Phenotypic specificity to enamel has focused research on genes encoding enamel-matrix proteins. We studied two families with autosomal-dominant hypocalcified AI and have identified nonsense mutations (R325X and Q398X) in the FAM83H gene on chromosome 8q24.3. The mutations perfectly cosegregate with the disease phenotype and demonstrate that FAM83H is required for proper dental-enamel calcification.
ISSN
0894-8275
Language
English
URI
https://hdl.handle.net/10371/48027
DOI
https://doi.org/10.1016/j.ajhg.2007.09.020.
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College of Dentistry/School of Dentistry (치과대학/치의학대학원)Dept. of Dentistry (치의학과)Journal Papers (저널논문_치의학과)
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