Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patients
Author:
Publisher
Wiley
Subject
General Dentistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0722.2001.00979.x/fullpdf
Reference23 articles.
1. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1);Lagerström;Genomics,1991
2. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta;Lagerström-Fermer;Genomics,1995
3. SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1);Lench;Hum Mol Genet,1994
4. An amelogenin gene defect associated with human X-linked amelogenesis imperfecta;Collier;Arch Oral Biol,1997
5. A novel gene expressed in rat ameloblasts codes for proteins with cell binding domains;Cerny;J Bone Miner Res,1996
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3. Evolutionary analysis of selective constraints identifies ameloblastin (AMBN) as a potential candidate for amelogenesis imperfecta;BMC Evolutionary Biology;2015-07-30
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