Amelogenesis Imperfecta in Two Families with Defined AMELX Deletions in ARHGAP6

Author:

Hu Jan C.-C.,Chan Hui-Chen,Simmer Stephen G.,Seymen Figen,Richardson Amelia S.,Hu Yuanyuan,Milkovich Rachel N.,Estrella Ninna M. R. P.,Yildirim Mine,Bayram Merve,Chen Chiung-Fen,Simmer James P.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference53 articles.

1. Witkop CJ Jr., Sauk JJ Jr. (1976) Heritable defects of enamel. In: Stewart RE, Prescott GH, editors. Oral Facial Genetics. St. Louis: C.V. Mosby Co. 151–226.

2. The molecular etiologies and associated phenotypes of amelogenesis imperfecta;JT Wright;Am J Med Genet A,2006

3. Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification;CJ Witkop Jr;J Oral Pathol,1989

4. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta;MH Rajpar;Hum Mol Genet,2001

5. FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta;JW Kim;Am J Hum Genet,2008

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