Article
Molecular characterization of amelogenesis imperfecta in Chinese patients.
Cells, tissues, organs - 1 Jan 2012
Song Y L, Wang C N, Zhang C Z, Yang K, Bian Z
Abstract excerpt
BACKGROUND: Mutations in 6 genes have been identified as being part of the etiology of amelogenesis imperfecta (AI) with various phenotypes in an isolated condition. Among them the FAM83H gene is the major contributor to the etiology of AI with unknown function. OBJECTIVE: This study aims to determine the phenotypic and molecular characterization of Chinese AI patients and to analyze the structure and function of...
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