Amelogenesis imperfecta phenotype–genotype correlations with two amelogenin gene mutations

The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes.

Eduardo Salido, P. H. Yen, K Koprivnikar et al. · PubMed · 1992 · 342 citations

Dentistry, Genetics, Molecular Genetics +14

Specific Amelogenin Gene Splice Products Have Signaling Effects on Cells in Culture and in Implants in Vivo

Arthur Veis, Kevin A. Tompkins, Keith Alvares et al. · Journal of Biological Chemistry · 2000 · 245 citations · Full text

Dentistry, Oral Biology, Dental Pulp Biology +16

An amelogenin gene defect associated with human X-linked amelogenesis imperfecta

Paul Collier, John J. Sauk, J. Rosenbloom et al. · Archives of Oral Biology · 1997 · 144 citations · Full text

Dentistry, Genetics, Molecular Genetics +12

Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)

Nicholas Lench, G B Winter · Human Mutation · 1995 · 127 citations

Dentistry, Genetics, Molecular Genetics +17

Unique Enamel Phenotype Associated with Amelogenin Gene (AMELX) Codon 41 Point Mutation

Darren B. Ravassipour, P. Suzanne Hart, Thomas C. Hart et al. · Journal of Dental Research · 2000 · 87 citations

Dentistry, Oral Biology, Craniofacial Genetics +16