Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation

D. B. Ravassipour, P. S. Hart, T. C. Hart, A. V. Ritter, M. Yamauchi, C. Gibson, J. T. Wright

Research output: Contribution to journalArticlepeer-review

Fingerprint

Dive into the research topics of 'Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology

Keyphrases