A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities
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DOI: 10.3389/fphys.2017.00333
Abstract: “Amelogenesis imperfecta” (AI) describes a group of genetic conditions that result in defects in tooth enamel formation. Mutations in many genes are known to cause AI, including the gene encoding the serine protease, kallikrein related… read more here.
Keywords: control; inner enamel; outer enamel; klk4 ... See more keywords