Characterization of Periodontal Structures of Enamelin-Null Mice
Author:
Publisher
Wiley
Subject
Periodontics
Link
http://www.joponline.org/doi/pdf/10.1902/jop.2013.120651
Reference27 articles.
1. Target gene analyses of 39 amelogenesis imperfecta kindreds
2. Altered Enamelin Phosphorylation Site Causes Amelogenesis Imperfecta
3. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta
4. Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature
5. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
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