A novel autosomal-recessive mutation,whitish chalk-like teeth, resembling amelogenesis imperfecta, maps to rat chromosome 14 corresponding to human 4q21
Author:
Publisher
Wiley
Subject
General Dentistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0722.2005.00254.x/fullpdf
Reference28 articles.
1. Amelogenesis imperfecta: a classification and catalogue for the 21st century;Aldred;Oral Dis,2003
2. Dental structural diseases mapping to human chromosome 4q21;Macdougall;Connect Tissue Res,2003
3. Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate;Downey;Eur J Hum Genet,2002
4. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1);Lagerström;Genomics,1991
5. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta;Rajpar;Hum Mol Genet,2001
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1. Positional and ultrastructural changes in peripheral pulp capillaries correlate with the active phase of dentin deposition and mineralization in rat molars;Journal of Oral Biosciences;2017-08
2. Regulation of Dental Enamel Shape and Hardness;Journal of Dental Research;2010-07-30
3. Rat wct mutation induces a hypo-mineralization form of amelogenesis imperfecta and cyst formation in molar teeth;Cell and Tissue Research;2007-08-21
4. Rat wct mutation prevents differentiation of maturation-stage ameloblasts resulting in hypo-mineralization in incisor teeth;Histochemistry and Cell Biology;2007-07-17
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